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AUBF- STRASINGER

AUBF- STRASINGER
100問 • 1年前
  • Yves Laure Pimentel
  • 通報

    問題一覧

  • 1

    A primary characteristic used to identify renal tubular epithelial cells is: A. Elongated structure B. Centrally located nucleus C. Spherical appearance

    D. Eccentrically located nucleus

  • 2

    Following an episode of hemoglobinuria, RTE cells may contain: A. Bilirubin B. Hemosiderin granules C. Porphobilinogen D. Myoglobin

    B. Hemosiderin granules

  • 3

    The predecessor of the oval fat body is the: A. Histiocyte B. Urothelial cell C. Monocyte D. Renal tubular cell

    D. Renal tubular cell

  • 4

    A structure believed to be an oval fat body produced a Maltese cross formation under polarized light but does not stain with Sudan III. The structure: A. Contains cholesterol B. Is not an oval fat body C. Contains neutral fats D. Is contaminated with immersion oil

    A. Contains cholesterol

  • 5

    The finding of yeast cells in the urine is commonly associated with: A. Cystitis B. Diabetes mellitus C. Pyelonephritis D. Liver disorders

    B. Diabetes mellitus

  • 6

    The primary component of urinary mucus is: A. Bence Jones protein B. Microalbumin C. Uromodulin D. Orthostatic protein

    C. Uromodulin

  • 7

    The majority of casts are formed in the: A. Proximal convoluted tubules B. Ascending loop of Henle C. Distal convoluted tubules D. Collecting ducts

    C. Distal convoluted tubules

  • 8

    Cylindruria refers to the presence of: A. Cylindrical renal tubular cells B. Mucus-resembling casts C. Hyaline and waxy casts D. All types of casts

    D. All types of casts

  • 9

    A person submitting a urine specimen following a strenuous exercise routine can normally have all of the following in the sediment except: A. Hyaline casts B. Granular casts C. RBC casts D. WBC casts

    D. WBC casts

  • 10

    Prior to identifying an RBC cast, all of the following should be observed except: A. Free-floating RBCs B. Intact RBCs in the cast C. Presence of a cast matrix D. A positive reagent strip blood reaction

    B. Intact RBCs in the cast

  • 11

    WBC casts are primarily associated with: A. Pyelonephritis B. Cystitis C. Glomerulonephritis D. Viral infections

    A. Pyelonephritis

  • 12

    The shape of the RTE cell associated with renal tubular epithelial casts is primarily: A. Elongated B. Cuboidal C. Round D. Columnar

    C. Round

  • 13

    When observing RTE casts, the cells are primarily: A. Embedded in a clear matrix B. Embedded in a granular matrix C. Attached to the surface of a matrix D. Stained by components of the urine filtrate

    A. Embedded in a clear matrix

  • 14

    The presence of fatty casts is associated with: A. Nephrotic syndrome B. Crush injuries C. Diabetes mellitus D. All of the above

    D. All of the above

  • 15

    Nonpathogenic granular casts contain: A. Cellular lysosomes B. Degenerated cells C. Protein aggregates D. Gram-positive cocci

    A. Cellular lysosomes

  • 16

    All of the following are true about waxy casts except they: A. Represent extreme urine stasis B. May have a brittle consistency C. Require staining to be visualized D. Contain degenerated granules

    C. Require staining to be visualized

  • 17

    Observation of broad casts represents: A. Destruction of tubular walls B. Dehydration and high fever C. Formation in the collecting ducts D. Both A and C

    D. Both A and C

  • 18

    All of the following contribute to urinary crystals formation except: A. Protein concentration B. pH C. Solute concentration D. Temperature

    A. Protein concentration

  • 19

    The most valuable initial aid for identifying crystals in a urine specimen is: A. pH B. Solubility C. Staining D. Polarized microscopy

    A. pH

  • 20

    Crystals associated with severe liver disease include all of the following except: A. Bilirubin B. Leucine C. Cystine D. Tyrosine

    C. Cystine

  • 21

    All of the following crystals routinely polarize except: A. Uric acid B. Cholesterol C. Radiographic dye D. Cystine

    D. Cystine

  • 22

    Casts and fibers can usually be differentiated using: A. Solubility characteristics B. Patient history C. Polarized light D. Fluorescent light

    C. Polarized light

  • 23

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Amorphous urates =

    Pink sediments

  • 24

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = Pink sediments

    Amorphous urates

  • 25

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = Yellow-brown

    Uric acid

  • 26

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Uric acid =

    Yellow-brown

  • 27

    Match the following crystals seen in acidic urine with their description/identifying characteristics: =Ovoid

    Calcium oxalate monohydrate

  • 28

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium oxalate monohydrate =

    Ovoid

  • 29

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium oxalate dihydrate =

    Envelope

  • 30

    Match the following crystals seen in acidic urine with their description/identifying characteristics: =Envelope

    Calcium oxalate dihydrate

  • 31

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = coffin lids

    Triple phosphate

  • 32

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Triple phosphate =

    coffin lids

  • 33

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = white precipitate

    Amorphous phosphate

  • 34

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Amorphous phosphate =

    white precipitate

  • 35

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium phosphate =

    thin prisms

  • 36

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = thin prisms

    Calcium phosphate

  • 37

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Ammonium biurate =

    thorny apples

  • 38

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = thorny apples

    Ammonium biurate

  • 39

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium carbonate =

    dumbbell shapes

  • 40

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = dumbbell shapes

    Calcium carbonate

  • 41

    Most glomerular disorders are caused by: A. Sudden drops in blood pressure B. Immunologic disorders C. Exposure to toxic substances D. Bacterial infections

    B. Immunologic disorders

  • 42

    Dysmorphic RBC casts would be a significant finding with all of the following except: A. Goodpasture syndrome B. Acute glomerulonephritis C. Chronic pyelonephritis D. Henoch-Schönlein purpura

    C. Chronic pyelonephritis

  • 43

    Occasional episodes of macroscopic hematuria over periods of 20 or more years are seen with: A. Crescentic glomerulonephritis B. IgA nephropathy C. Nephrotic syndrome D. Wegener granulomatosis

    B. IgA nephropathy

  • 44

    Antiglomerular basement membrane antibody is seen with: A. Wegener granulomatosis B. IgA nephropathy C. Goodpasture syndrome D. Diabetic nephropathy

    C. Goodpasture syndrome

  • 45

    Antineutrophilic cytoplasmic antibody is diagnostic for: A. IgA nephropathy B. Wegener granulomatosis C. Henoch-Schönlein purpura D. Goodpasture syndrome

    B. Wegener granulomatosis

  • 46

    Respiratory and renal symptoms are associated with all of the following except: A. IgA nephropathy B. Wegener granulomatosis C. Henoch-Schönlein purpura D. Goodpasture syndrome

    D. Goodpasture syndrome

  • 47

    The presence of fatty casts is associated with all of the following except: A. Nephrotic syndrome B. Focal segmental glomerulosclerosis C. Nephrogenic diabetes insipidus D. Minimal change disease

    C. Nephrogenic diabetes insipidus

  • 48

    The highest levels of proteinuria are seen with: A. Alport syndrome B. Diabetic nephropathy C. IgA nephropathy D. Nephrotic syndrome

    D. Nephrotic syndrome

  • 49

    Ischemia frequently produces: A. Acute renal tubular necrosis B. Minimal change disorder C. Renal glycosuria D. Goodpasture’s syndrome

    A. Acute renal tubular necrosis

  • 50

    A disorder associated with polyuria and low specific gravity is: A. Renal glucosuria B. Minimal change disease C. Nephrogenic diabetes insipidus D. Focal segmental glomerulosclerosis

    C. Nephrogenic diabetes insipidus

  • 51

    An inherited disorder producing a generalized defect in tubular reabsorption is: A. Alport syndrome B. Acute interstitial nephritis C. Fanconi syndrome D. Renal glycosuria

    C. Fanconi syndrome

  • 52

    A teenage boy who develops gout in his big toe and has a high serum uric acid should be monitored for: A. Fanconi syndrome B. Renal calculi C. Uromodulin-associated kidney disease D. Chronic interstitial nephritis

    C. Uromodulin-associated kidney disease

  • 53

    The only protein produced by the kidney is: A. Albumin B. Uromodulin C. Uroprotein D. Globulin

    B. Uromodulin

  • 54

    The presence of renal tubular epithelial cells and casts is an indication of: A. Acute interstitial nephritis B. Chronic glomerulonephritis C. Minimal change disease D. Acute tubular necrosis

    D. Acute tubular necrosis

  • 55

    Differentiation between cystitis and pyelonephritis is aided by the presence of: A. WBC casts B. RBC casts C. Bacteria D. Granular casts

    A. WBC casts

  • 56

    The presence of WBCs and WBC casts with no bacteria is indicative of: A. Chronic pyelonephritis B. Acute tubular necrosis C. Acute interstitial nephritis D. Both B and C

    C. Acute interstitial nephritis

  • 57

    End-stage renal disease is characterized by all of the following except: A. Hypersthenuria B. Isosthenuria C. Azotemia D. Electrolyte imbalance

    A. Hypersthenuria

  • 58

    Prerenal acute renal failure could be caused by: A. Massive hemorrhage B. Acute tubular necrosis C. Acute interstitial nephritis D. Malignant tumors

    A. Massive hemorrhage

  • 59

    The most common composition of renal calculi is: A. Calcium oxalate B. Magnesium ammonium phosphate C. Cystine D. Uric acid

    A. Calcium oxalate

  • 60

    Urinalysis on a patient with severe back pain being evaluated for renal calculi would be most beneficial if it showed: A. Heavy proteinuria B. Low specific gravity C. Uric acid crystals D. Microscopic hematuria

    D. Microscopic hematuria

  • 61

    All states require newborn screening for PKU for early: A. Modifications of diet B. Administration of antibiotics C. Detection of diabetes D. Initiation of gene therapy

    A. Modifications of diet

  • 62

    All of the following disorders can be detected by newborn screening except: A. Tyrosyluria B. MSUD C. Melanuria D. Galactosemia

    C. Melanuria

  • 63

    The best specimen for early newborn screening is a: A. Timed urine specimen B. Blood specimen C. First morning urine specimen D. Fecal specimen

    B. Blood specimen

  • 64

    Abnormal urine screening tests categorized as an overflow disorder include all of the following except: A. Alkaptonuria B. Galactosemia C. Melanuria D. Cystinuria

    C. Melanuria

  • 65

    Which of the following disorders is not associated with the phenylalanine-tyrosine pathway? A. MSUD B. Alkaptonuria C. Albinism D. Tyrosinemia

    A. MSUD

  • 66

    The least serious form of tyrosylemia is: A. Immature liver function B. Type 1 C. Type 2 D. Type 3

    A. Immature liver function

  • 67

    An overflow disorder of the phenylalanine-tyrosine pathway that would produce a positive reaction with the reagent strip test for ketones is: A. Alkaptonuria B. Melanuria C. MSUD D. Tyrosyluria

    C. MSUD

  • 68

    An overflow disorder that could produce a false- positive reaction with Clinitest procedure is: A. Cystinuria B. Alkaptonuria C. Indicanuria D. Porphyrinuria

    B. Alkaptonuria

  • 69

    9. A urine that turns black after sitting by the sink for several hours could be indicative of: A. Alkaptonuria B. MSUD C. Melanuria D. Both A and C

    D. Both A and C

  • 70

    Ketonuria in a newborn is an indication of: A. MSUD B. Isovaleric acidemia C. Methylmalonic acidemia D. All of the above

    D. All of the above

  • 71

    Urine from a newborn with MSUD will have a significant: A. Pale color B. Yellow precipitate C. Milky appearance D. Sweet odor

    D. Sweet odor

  • 72

    Hartnup disease is a disorder associated with the metabolism of: A. Organic acids B. Tryptophan C. Cystine D. Phenylalanine

    B. Tryptophan

  • 73

    5-HIAA is a degradation product of: A. Heme B. Indole C. Serotonin D. Melanin

    C. Serotonin

  • 74

    Elevated urinary levels of 5-HIAA are associated with: A. Carcinoid tumors B. Hartnup disease C. Cystinuria D. Platelet disorders

    A. Carcinoid tumors

  • 75

    False-positive levels of 5-HIAA can be caused by a diet high in: A. Meat B. Carbohydrates C. Starch D. Bananas

    D. Bananas

  • 76

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis IEM

    B. Cystinosis

  • 77

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Fanconi syndrome

    B. Cystinosis

  • 78

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Cystine deposits in the cornea

    B. Cystinosis

  • 79

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Inherited disorder of tubular reabsorption

    A. Cystinuria

  • 80

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Early renal calculi formation

    A. Cystinuria

  • 81

    Blue diaper syndrome is associated with: A. Lesch-Nyhan syndrome B. Phenylketonuria C. Cystinuria D. Hartnup disease

    D. Hartnup disease

  • 82

    Homocystinuria is caused by failure to metabolize: A. Lysine B. Methionine C. Arginine D. Cystine

    B. Methionine

  • 83

    The Ehrlich reaction will only detect the presence of: A. Uroporphyrin B. Porphobilinogen C. Coproporphyrin D. Protoporphyrin

    B. Porphobilinogen

  • 84

    Acetyl acetone is added to the urine before performing the Ehrlich test when checking for: A. Aminolevulinic acid B. Porphobilinogen C. Uroporphyrin D. Coproporphyrin

    B. Porphobilinogen

  • 85

    The classic urine color associated with porphyria is: A. Dark yellow B. Indigo blue C. Pink D. Port wine

    D. Port wine

  • 86

    Which of the following specimens can be used for porphyrin testing? A. Urine B. Blood C. Feces D. All of the above

    D. All of the above

  • 87

    The two stages of heme formation affected by lead poisoning are: A. Porphobilinogen and uroporphyrin B. Aminolevulinic acid and porphobilinogen C. Coproporphyrin and protoporphyrin D. Aminolevulinic acid and protoporphyrin

    D. Aminolevulinic acid and protoporphyrin

  • 88

    Hurler, Hunter, and Sanfilippo syndromes are hereditary disorders affecting metabolism of: A. Porphyrins B. Purines C. Mucopolysaccharides D. Tryptophan

    C. Mucopolysaccharides

  • 89

    Many uric acid crystals in a pediatric urine specimen may indicate: A. Hurler syndrome B. Lesch-Nyhan disease C. Melituria D. Sanfilippo syndrome

    B. Lesch-Nyhan disease

  • 90

    Deficiency of the GALT enzyme will produce a: A. Positive Clinitest B. Glycosuria C. Galactosemia D. Both A and C

    D. Both A and C

  • 91

    Match the metabolic urine disorders with their classic urine abnormalities. 1. Cystinuria 2. PKU 3. Indicanuria 4. Alkaptonuria 5. Lesch-Nyhan disease 6. Isovaleric academia A. Sulfur odor B. Sweaty feet odor C. Orange sand in diaper D. Mousy odor E. Black color F. Blue color

    _A_ _D_ _F_ _E_ _C_ _B_

  • 92

    The functions of the CSF include all of the following except: A. Removing metabolic wastes B. Producing an ultrafiltrate of plasma C. Supplying nutrients to the CNS D. Protecting the brain and spinal cord

    B. Producing an ultrafiltrate of plasma

  • 93

    The CSF flows through the: A. Choroid plexus B. Pia mater C. Arachnoid space D. Dura mater

    C. Arachnoid space

  • 94

    Substances present in the CSF are controlled by the: A. Arachnoid granulations B. Blood–brain barrier C. Presence of one-way valves D. Blood–CSF barrier

    B. Blood–brain barrier

  • 95

    What department is the CSF tube labeled 3 routinely sent to? A. Hematology B. Chemistry C. Microbiology D. Serology

    A. Hematology

  • 96

    The CSF tube that should be kept at room temperature is: A. Tube 1 B. Tube 2 C. Tube 3 D. Tube 4

    B. Tube 2

  • 97

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Even distribution of blood in all tubes

    B. Intracranial hemorrhage

  • 98

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Xanthochromic supernatant

    B. Intracranial hemorrhage

  • 99

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Concentration of blood in tube 1 is greater than in tube 3

    A. Traumatic tap

  • 100

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Specimen contains clots

    A. Traumatic tap

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    GLYCOGEN STORAGE DISEASES

    GLYCOGEN STORAGE DISEASES

    17問 • 2年前
    Yves Laure Pimentel

    LIPID STORAGE DISEASES

    LIPID STORAGE DISEASES

    Yves Laure Pimentel · 14問 · 2年前

    LIPID STORAGE DISEASES

    LIPID STORAGE DISEASES

    14問 • 2年前
    Yves Laure Pimentel

    PROTEINS

    PROTEINS

    Yves Laure Pimentel · 71問 · 2年前

    PROTEINS

    PROTEINS

    71問 • 2年前
    Yves Laure Pimentel

    QUICK FIRE- ELECTRODES

    QUICK FIRE- ELECTRODES

    Yves Laure Pimentel · 7問 · 2年前

    QUICK FIRE- ELECTRODES

    QUICK FIRE- ELECTRODES

    7問 • 2年前
    Yves Laure Pimentel

    ELECTROLYTES

    ELECTROLYTES

    Yves Laure Pimentel · 10問 · 2年前

    ELECTROLYTES

    ELECTROLYTES

    10問 • 2年前
    Yves Laure Pimentel

    DRUGS

    DRUGS

    Yves Laure Pimentel · 27問 · 2年前

    DRUGS

    DRUGS

    27問 • 2年前
    Yves Laure Pimentel

    TOXIC AGENTS:

    TOXIC AGENTS:

    Yves Laure Pimentel · 12問 · 2年前

    TOXIC AGENTS:

    TOXIC AGENTS:

    12問 • 2年前
    Yves Laure Pimentel

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    Yves Laure Pimentel · 100問 · 2年前

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    100問 • 2年前
    Yves Laure Pimentel

    HEMATOLOGY (HEMATOPOIESIS 2)

    HEMATOLOGY (HEMATOPOIESIS 2)

    Yves Laure Pimentel · 29問 · 2年前

    HEMATOLOGY (HEMATOPOIESIS 2)

    HEMATOLOGY (HEMATOPOIESIS 2)

    29問 • 2年前
    Yves Laure Pimentel

    hema diseases

    hema diseases

    Yves Laure Pimentel · 25問 · 2年前

    hema diseases

    hema diseases

    25問 • 2年前
    Yves Laure Pimentel

    AML

    AML

    Yves Laure Pimentel · 43問 · 2年前

    AML

    AML

    43問 • 2年前
    Yves Laure Pimentel

    GLOBIN SYNTHESIS

    GLOBIN SYNTHESIS

    Yves Laure Pimentel · 71問 · 2年前

    GLOBIN SYNTHESIS

    GLOBIN SYNTHESIS

    71問 • 2年前
    Yves Laure Pimentel

    HEMATOLOGY REFERENCE RANGES

    HEMATOLOGY REFERENCE RANGES

    Yves Laure Pimentel · 31問 · 2年前

    HEMATOLOGY REFERENCE RANGES

    HEMATOLOGY REFERENCE RANGES

    31問 • 2年前
    Yves Laure Pimentel

    DISORDERS OF PRIMARY HEMOSTASIS

    DISORDERS OF PRIMARY HEMOSTASIS

    Yves Laure Pimentel · 34問 · 2年前

    DISORDERS OF PRIMARY HEMOSTASIS

    DISORDERS OF PRIMARY HEMOSTASIS

    34問 • 2年前
    Yves Laure Pimentel

    PLATELET DISORDERS

    PLATELET DISORDERS

    Yves Laure Pimentel · 37問 · 2年前

    PLATELET DISORDERS

    PLATELET DISORDERS

    37問 • 2年前
    Yves Laure Pimentel

    CHARACTERISTICS OF CLOTTING FACTORS

    CHARACTERISTICS OF CLOTTING FACTORS

    Yves Laure Pimentel · 100問 · 2年前

    CHARACTERISTICS OF CLOTTING FACTORS

    CHARACTERISTICS OF CLOTTING FACTORS

    100問 • 2年前
    Yves Laure Pimentel

    4. CLASSIFICATION OF MACROPHAGE

    4. CLASSIFICATION OF MACROPHAGE

    Yves Laure Pimentel · 12問 · 2年前

    4. CLASSIFICATION OF MACROPHAGE

    4. CLASSIFICATION OF MACROPHAGE

    12問 • 2年前
    Yves Laure Pimentel

    3. NATURAL OR INNATE IMMUNITY

    3. NATURAL OR INNATE IMMUNITY

    Yves Laure Pimentel · 39問 · 2年前

    3. NATURAL OR INNATE IMMUNITY

    3. NATURAL OR INNATE IMMUNITY

    39問 • 2年前
    Yves Laure Pimentel

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    Yves Laure Pimentel · 55問 · 2年前

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    55問 • 2年前
    Yves Laure Pimentel

    6. PHAGOCYTOSIS Chemotaxis

    6. PHAGOCYTOSIS Chemotaxis

    Yves Laure Pimentel · 37問 · 2年前

    6. PHAGOCYTOSIS Chemotaxis

    6. PHAGOCYTOSIS Chemotaxis

    37問 • 2年前
    Yves Laure Pimentel

    8. NATURE OF ANTIGEN

    8. NATURE OF ANTIGEN

    Yves Laure Pimentel · 44問 · 2年前

    8. NATURE OF ANTIGEN

    8. NATURE OF ANTIGEN

    44問 • 2年前
    Yves Laure Pimentel

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    Yves Laure Pimentel · 50問 · 2年前

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    50問 • 2年前
    Yves Laure Pimentel

    1. HISTORY

    1. HISTORY

    Yves Laure Pimentel · 69問 · 2年前

    1. HISTORY

    1. HISTORY

    69問 • 2年前
    Yves Laure Pimentel

    2. TYPES OF IMMUNITY

    2. TYPES OF IMMUNITY

    Yves Laure Pimentel · 38問 · 2年前

    2. TYPES OF IMMUNITY

    2. TYPES OF IMMUNITY

    38問 • 2年前
    Yves Laure Pimentel

    7. PHAGOCYTOSIS Engulfment and Digestion

    7. PHAGOCYTOSIS Engulfment and Digestion

    Yves Laure Pimentel · 21問 · 2年前

    7. PHAGOCYTOSIS Engulfment and Digestion

    7. PHAGOCYTOSIS Engulfment and Digestion

    21問 • 2年前
    Yves Laure Pimentel

    8. PHAGOCYTOSIS EXOCYTOSIS

    8. PHAGOCYTOSIS EXOCYTOSIS

    Yves Laure Pimentel · 15問 · 2年前

    8. PHAGOCYTOSIS EXOCYTOSIS

    8. PHAGOCYTOSIS EXOCYTOSIS

    15問 • 2年前
    Yves Laure Pimentel

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    Yves Laure Pimentel · 32問 · 2年前

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    32問 • 2年前
    Yves Laure Pimentel

    11. TRANSPLANTATION IMMUNOLOGY

    11. TRANSPLANTATION IMMUNOLOGY

    Yves Laure Pimentel · 30問 · 2年前

    11. TRANSPLANTATION IMMUNOLOGY

    11. TRANSPLANTATION IMMUNOLOGY

    30問 • 2年前
    Yves Laure Pimentel

    2. LYMPHOID ORGANS

    2. LYMPHOID ORGANS

    Yves Laure Pimentel · 38問 · 2年前

    2. LYMPHOID ORGANS

    2. LYMPHOID ORGANS

    38問 • 2年前
    Yves Laure Pimentel

    3. CLUSTER OF DIFFERENTIATION

    3. CLUSTER OF DIFFERENTIATION

    Yves Laure Pimentel · 48問 · 2年前

    3. CLUSTER OF DIFFERENTIATION

    3. CLUSTER OF DIFFERENTIATION

    48問 • 2年前
    Yves Laure Pimentel

    4. T-CELL DIFFERENTIATION

    4. T-CELL DIFFERENTIATION

    Yves Laure Pimentel · 35問 · 2年前

    4. T-CELL DIFFERENTIATION

    4. T-CELL DIFFERENTIATION

    35問 • 2年前
    Yves Laure Pimentel

    5. T CELL IMMUNODEFICIENCIES

    5. T CELL IMMUNODEFICIENCIES

    Yves Laure Pimentel · 18問 · 2年前

    5. T CELL IMMUNODEFICIENCIES

    5. T CELL IMMUNODEFICIENCIES

    18問 • 2年前
    Yves Laure Pimentel

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    Yves Laure Pimentel · 44問 · 2年前

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    44問 • 2年前
    Yves Laure Pimentel

    7. B CELL IMMUNODEFICIENCIES

    7. B CELL IMMUNODEFICIENCIES

    Yves Laure Pimentel · 23問 · 2年前

    7. B CELL IMMUNODEFICIENCIES

    7. B CELL IMMUNODEFICIENCIES

    23問 • 2年前
    Yves Laure Pimentel

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    Yves Laure Pimentel · 34問 · 2年前

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    34問 • 2年前
    Yves Laure Pimentel

    9. COMPARISON OF T AND B CELLS

    9. COMPARISON OF T AND B CELLS

    Yves Laure Pimentel · 12問 · 2年前

    9. COMPARISON OF T AND B CELLS

    9. COMPARISON OF T AND B CELLS

    12問 • 2年前
    Yves Laure Pimentel

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    Yves Laure Pimentel · 16問 · 2年前

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    16問 • 2年前
    Yves Laure Pimentel

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    Yves Laure Pimentel · 15問 · 2年前

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    15問 • 2年前
    Yves Laure Pimentel

    12. ANTIBODY

    12. ANTIBODY

    Yves Laure Pimentel · 79問 · 2年前

    12. ANTIBODY

    12. ANTIBODY

    79問 • 2年前
    Yves Laure Pimentel

    13. TYPES OF ANTIBODIES

    13. TYPES OF ANTIBODIES

    Yves Laure Pimentel · 97問 · 2年前

    13. TYPES OF ANTIBODIES

    13. TYPES OF ANTIBODIES

    97問 • 2年前
    Yves Laure Pimentel

    14. MONOCLONAL ANTIBODIES

    14. MONOCLONAL ANTIBODIES

    Yves Laure Pimentel · 11問 · 2年前

    14. MONOCLONAL ANTIBODIES

    14. MONOCLONAL ANTIBODIES

    11問 • 2年前
    Yves Laure Pimentel

    1. INTERLEUKINS

    1. INTERLEUKINS

    Yves Laure Pimentel · 23問 · 2年前

    1. INTERLEUKINS

    1. INTERLEUKINS

    23問 • 2年前
    Yves Laure Pimentel

    2. INTERFERONS

    2. INTERFERONS

    Yves Laure Pimentel · 28問 · 2年前

    2. INTERFERONS

    2. INTERFERONS

    28問 • 2年前
    Yves Laure Pimentel

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    Yves Laure Pimentel · 8問 · 2年前

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    8問 • 2年前
    Yves Laure Pimentel

    4. COMPLEMENT SYSTEM

    4. COMPLEMENT SYSTEM

    Yves Laure Pimentel · 19問 · 2年前

    4. COMPLEMENT SYSTEM

    4. COMPLEMENT SYSTEM

    19問 • 2年前
    Yves Laure Pimentel

    15. COMPLEMENT SYSTEM

    15. COMPLEMENT SYSTEM

    Yves Laure Pimentel · 76問 · 2年前

    15. COMPLEMENT SYSTEM

    15. COMPLEMENT SYSTEM

    76問 • 2年前
    Yves Laure Pimentel

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    Yves Laure Pimentel · 21問 · 2年前

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    21問 • 2年前
    Yves Laure Pimentel

    17. COMPLEMENT AND DISEASE STATES

    17. COMPLEMENT AND DISEASE STATES

    Yves Laure Pimentel · 29問 · 2年前

    17. COMPLEMENT AND DISEASE STATES

    17. COMPLEMENT AND DISEASE STATES

    29問 • 2年前
    Yves Laure Pimentel

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    Yves Laure Pimentel · 19問 · 2年前

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    19問 • 2年前
    Yves Laure Pimentel

    19. CYTOKINES

    19. CYTOKINES

    Yves Laure Pimentel · 22問 · 2年前

    19. CYTOKINES

    19. CYTOKINES

    22問 • 2年前
    Yves Laure Pimentel

    20. INTERLEUKINS

    20. INTERLEUKINS

    Yves Laure Pimentel · 24問 · 2年前

    20. INTERLEUKINS

    20. INTERLEUKINS

    24問 • 2年前
    Yves Laure Pimentel

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    Yves Laure Pimentel · 21問 · 2年前

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    21問 • 2年前
    Yves Laure Pimentel

    1. SERO

    1. SERO

    Yves Laure Pimentel · 54問 · 2年前

    1. SERO

    1. SERO

    54問 • 2年前
    Yves Laure Pimentel

    2. PRECIPITATION

    2. PRECIPITATION

    Yves Laure Pimentel · 38問 · 2年前

    2. PRECIPITATION

    2. PRECIPITATION

    38問 • 2年前
    Yves Laure Pimentel

    3. PASSIVE IMMUNODIFFUSION

    3. PASSIVE IMMUNODIFFUSION

    Yves Laure Pimentel · 17問 · 2年前

    3. PASSIVE IMMUNODIFFUSION

    3. PASSIVE IMMUNODIFFUSION

    17問 • 2年前
    Yves Laure Pimentel

    4. OUCHTERLONY

    4. OUCHTERLONY

    Yves Laure Pimentel · 15問 · 2年前

    4. OUCHTERLONY

    4. OUCHTERLONY

    15問 • 2年前
    Yves Laure Pimentel

    5. ELECTROPHORETIC TECHNIQUE

    5. ELECTROPHORETIC TECHNIQUE

    Yves Laure Pimentel · 9問 · 2年前

    5. ELECTROPHORETIC TECHNIQUE

    5. ELECTROPHORETIC TECHNIQUE

    9問 • 2年前
    Yves Laure Pimentel

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    Yves Laure Pimentel · 11問 · 2年前

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    11問 • 2年前
    Yves Laure Pimentel

    7. IMMUNOFIXATION ELECTROPHORESIS

    7. IMMUNOFIXATION ELECTROPHORESIS

    Yves Laure Pimentel · 29問 · 2年前

    7. IMMUNOFIXATION ELECTROPHORESIS

    7. IMMUNOFIXATION ELECTROPHORESIS

    29問 • 2年前
    Yves Laure Pimentel

    問題一覧

  • 1

    A primary characteristic used to identify renal tubular epithelial cells is: A. Elongated structure B. Centrally located nucleus C. Spherical appearance

    D. Eccentrically located nucleus

  • 2

    Following an episode of hemoglobinuria, RTE cells may contain: A. Bilirubin B. Hemosiderin granules C. Porphobilinogen D. Myoglobin

    B. Hemosiderin granules

  • 3

    The predecessor of the oval fat body is the: A. Histiocyte B. Urothelial cell C. Monocyte D. Renal tubular cell

    D. Renal tubular cell

  • 4

    A structure believed to be an oval fat body produced a Maltese cross formation under polarized light but does not stain with Sudan III. The structure: A. Contains cholesterol B. Is not an oval fat body C. Contains neutral fats D. Is contaminated with immersion oil

    A. Contains cholesterol

  • 5

    The finding of yeast cells in the urine is commonly associated with: A. Cystitis B. Diabetes mellitus C. Pyelonephritis D. Liver disorders

    B. Diabetes mellitus

  • 6

    The primary component of urinary mucus is: A. Bence Jones protein B. Microalbumin C. Uromodulin D. Orthostatic protein

    C. Uromodulin

  • 7

    The majority of casts are formed in the: A. Proximal convoluted tubules B. Ascending loop of Henle C. Distal convoluted tubules D. Collecting ducts

    C. Distal convoluted tubules

  • 8

    Cylindruria refers to the presence of: A. Cylindrical renal tubular cells B. Mucus-resembling casts C. Hyaline and waxy casts D. All types of casts

    D. All types of casts

  • 9

    A person submitting a urine specimen following a strenuous exercise routine can normally have all of the following in the sediment except: A. Hyaline casts B. Granular casts C. RBC casts D. WBC casts

    D. WBC casts

  • 10

    Prior to identifying an RBC cast, all of the following should be observed except: A. Free-floating RBCs B. Intact RBCs in the cast C. Presence of a cast matrix D. A positive reagent strip blood reaction

    B. Intact RBCs in the cast

  • 11

    WBC casts are primarily associated with: A. Pyelonephritis B. Cystitis C. Glomerulonephritis D. Viral infections

    A. Pyelonephritis

  • 12

    The shape of the RTE cell associated with renal tubular epithelial casts is primarily: A. Elongated B. Cuboidal C. Round D. Columnar

    C. Round

  • 13

    When observing RTE casts, the cells are primarily: A. Embedded in a clear matrix B. Embedded in a granular matrix C. Attached to the surface of a matrix D. Stained by components of the urine filtrate

    A. Embedded in a clear matrix

  • 14

    The presence of fatty casts is associated with: A. Nephrotic syndrome B. Crush injuries C. Diabetes mellitus D. All of the above

    D. All of the above

  • 15

    Nonpathogenic granular casts contain: A. Cellular lysosomes B. Degenerated cells C. Protein aggregates D. Gram-positive cocci

    A. Cellular lysosomes

  • 16

    All of the following are true about waxy casts except they: A. Represent extreme urine stasis B. May have a brittle consistency C. Require staining to be visualized D. Contain degenerated granules

    C. Require staining to be visualized

  • 17

    Observation of broad casts represents: A. Destruction of tubular walls B. Dehydration and high fever C. Formation in the collecting ducts D. Both A and C

    D. Both A and C

  • 18

    All of the following contribute to urinary crystals formation except: A. Protein concentration B. pH C. Solute concentration D. Temperature

    A. Protein concentration

  • 19

    The most valuable initial aid for identifying crystals in a urine specimen is: A. pH B. Solubility C. Staining D. Polarized microscopy

    A. pH

  • 20

    Crystals associated with severe liver disease include all of the following except: A. Bilirubin B. Leucine C. Cystine D. Tyrosine

    C. Cystine

  • 21

    All of the following crystals routinely polarize except: A. Uric acid B. Cholesterol C. Radiographic dye D. Cystine

    D. Cystine

  • 22

    Casts and fibers can usually be differentiated using: A. Solubility characteristics B. Patient history C. Polarized light D. Fluorescent light

    C. Polarized light

  • 23

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Amorphous urates =

    Pink sediments

  • 24

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = Pink sediments

    Amorphous urates

  • 25

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = Yellow-brown

    Uric acid

  • 26

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Uric acid =

    Yellow-brown

  • 27

    Match the following crystals seen in acidic urine with their description/identifying characteristics: =Ovoid

    Calcium oxalate monohydrate

  • 28

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium oxalate monohydrate =

    Ovoid

  • 29

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium oxalate dihydrate =

    Envelope

  • 30

    Match the following crystals seen in acidic urine with their description/identifying characteristics: =Envelope

    Calcium oxalate dihydrate

  • 31

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = coffin lids

    Triple phosphate

  • 32

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Triple phosphate =

    coffin lids

  • 33

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = white precipitate

    Amorphous phosphate

  • 34

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Amorphous phosphate =

    white precipitate

  • 35

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium phosphate =

    thin prisms

  • 36

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = thin prisms

    Calcium phosphate

  • 37

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Ammonium biurate =

    thorny apples

  • 38

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = thorny apples

    Ammonium biurate

  • 39

    Match the following crystals seen in acidic urine with their description/identifying characteristics: Calcium carbonate =

    dumbbell shapes

  • 40

    Match the following crystals seen in acidic urine with their description/identifying characteristics: = dumbbell shapes

    Calcium carbonate

  • 41

    Most glomerular disorders are caused by: A. Sudden drops in blood pressure B. Immunologic disorders C. Exposure to toxic substances D. Bacterial infections

    B. Immunologic disorders

  • 42

    Dysmorphic RBC casts would be a significant finding with all of the following except: A. Goodpasture syndrome B. Acute glomerulonephritis C. Chronic pyelonephritis D. Henoch-Schönlein purpura

    C. Chronic pyelonephritis

  • 43

    Occasional episodes of macroscopic hematuria over periods of 20 or more years are seen with: A. Crescentic glomerulonephritis B. IgA nephropathy C. Nephrotic syndrome D. Wegener granulomatosis

    B. IgA nephropathy

  • 44

    Antiglomerular basement membrane antibody is seen with: A. Wegener granulomatosis B. IgA nephropathy C. Goodpasture syndrome D. Diabetic nephropathy

    C. Goodpasture syndrome

  • 45

    Antineutrophilic cytoplasmic antibody is diagnostic for: A. IgA nephropathy B. Wegener granulomatosis C. Henoch-Schönlein purpura D. Goodpasture syndrome

    B. Wegener granulomatosis

  • 46

    Respiratory and renal symptoms are associated with all of the following except: A. IgA nephropathy B. Wegener granulomatosis C. Henoch-Schönlein purpura D. Goodpasture syndrome

    D. Goodpasture syndrome

  • 47

    The presence of fatty casts is associated with all of the following except: A. Nephrotic syndrome B. Focal segmental glomerulosclerosis C. Nephrogenic diabetes insipidus D. Minimal change disease

    C. Nephrogenic diabetes insipidus

  • 48

    The highest levels of proteinuria are seen with: A. Alport syndrome B. Diabetic nephropathy C. IgA nephropathy D. Nephrotic syndrome

    D. Nephrotic syndrome

  • 49

    Ischemia frequently produces: A. Acute renal tubular necrosis B. Minimal change disorder C. Renal glycosuria D. Goodpasture’s syndrome

    A. Acute renal tubular necrosis

  • 50

    A disorder associated with polyuria and low specific gravity is: A. Renal glucosuria B. Minimal change disease C. Nephrogenic diabetes insipidus D. Focal segmental glomerulosclerosis

    C. Nephrogenic diabetes insipidus

  • 51

    An inherited disorder producing a generalized defect in tubular reabsorption is: A. Alport syndrome B. Acute interstitial nephritis C. Fanconi syndrome D. Renal glycosuria

    C. Fanconi syndrome

  • 52

    A teenage boy who develops gout in his big toe and has a high serum uric acid should be monitored for: A. Fanconi syndrome B. Renal calculi C. Uromodulin-associated kidney disease D. Chronic interstitial nephritis

    C. Uromodulin-associated kidney disease

  • 53

    The only protein produced by the kidney is: A. Albumin B. Uromodulin C. Uroprotein D. Globulin

    B. Uromodulin

  • 54

    The presence of renal tubular epithelial cells and casts is an indication of: A. Acute interstitial nephritis B. Chronic glomerulonephritis C. Minimal change disease D. Acute tubular necrosis

    D. Acute tubular necrosis

  • 55

    Differentiation between cystitis and pyelonephritis is aided by the presence of: A. WBC casts B. RBC casts C. Bacteria D. Granular casts

    A. WBC casts

  • 56

    The presence of WBCs and WBC casts with no bacteria is indicative of: A. Chronic pyelonephritis B. Acute tubular necrosis C. Acute interstitial nephritis D. Both B and C

    C. Acute interstitial nephritis

  • 57

    End-stage renal disease is characterized by all of the following except: A. Hypersthenuria B. Isosthenuria C. Azotemia D. Electrolyte imbalance

    A. Hypersthenuria

  • 58

    Prerenal acute renal failure could be caused by: A. Massive hemorrhage B. Acute tubular necrosis C. Acute interstitial nephritis D. Malignant tumors

    A. Massive hemorrhage

  • 59

    The most common composition of renal calculi is: A. Calcium oxalate B. Magnesium ammonium phosphate C. Cystine D. Uric acid

    A. Calcium oxalate

  • 60

    Urinalysis on a patient with severe back pain being evaluated for renal calculi would be most beneficial if it showed: A. Heavy proteinuria B. Low specific gravity C. Uric acid crystals D. Microscopic hematuria

    D. Microscopic hematuria

  • 61

    All states require newborn screening for PKU for early: A. Modifications of diet B. Administration of antibiotics C. Detection of diabetes D. Initiation of gene therapy

    A. Modifications of diet

  • 62

    All of the following disorders can be detected by newborn screening except: A. Tyrosyluria B. MSUD C. Melanuria D. Galactosemia

    C. Melanuria

  • 63

    The best specimen for early newborn screening is a: A. Timed urine specimen B. Blood specimen C. First morning urine specimen D. Fecal specimen

    B. Blood specimen

  • 64

    Abnormal urine screening tests categorized as an overflow disorder include all of the following except: A. Alkaptonuria B. Galactosemia C. Melanuria D. Cystinuria

    C. Melanuria

  • 65

    Which of the following disorders is not associated with the phenylalanine-tyrosine pathway? A. MSUD B. Alkaptonuria C. Albinism D. Tyrosinemia

    A. MSUD

  • 66

    The least serious form of tyrosylemia is: A. Immature liver function B. Type 1 C. Type 2 D. Type 3

    A. Immature liver function

  • 67

    An overflow disorder of the phenylalanine-tyrosine pathway that would produce a positive reaction with the reagent strip test for ketones is: A. Alkaptonuria B. Melanuria C. MSUD D. Tyrosyluria

    C. MSUD

  • 68

    An overflow disorder that could produce a false- positive reaction with Clinitest procedure is: A. Cystinuria B. Alkaptonuria C. Indicanuria D. Porphyrinuria

    B. Alkaptonuria

  • 69

    9. A urine that turns black after sitting by the sink for several hours could be indicative of: A. Alkaptonuria B. MSUD C. Melanuria D. Both A and C

    D. Both A and C

  • 70

    Ketonuria in a newborn is an indication of: A. MSUD B. Isovaleric acidemia C. Methylmalonic acidemia D. All of the above

    D. All of the above

  • 71

    Urine from a newborn with MSUD will have a significant: A. Pale color B. Yellow precipitate C. Milky appearance D. Sweet odor

    D. Sweet odor

  • 72

    Hartnup disease is a disorder associated with the metabolism of: A. Organic acids B. Tryptophan C. Cystine D. Phenylalanine

    B. Tryptophan

  • 73

    5-HIAA is a degradation product of: A. Heme B. Indole C. Serotonin D. Melanin

    C. Serotonin

  • 74

    Elevated urinary levels of 5-HIAA are associated with: A. Carcinoid tumors B. Hartnup disease C. Cystinuria D. Platelet disorders

    A. Carcinoid tumors

  • 75

    False-positive levels of 5-HIAA can be caused by a diet high in: A. Meat B. Carbohydrates C. Starch D. Bananas

    D. Bananas

  • 76

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis IEM

    B. Cystinosis

  • 77

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Fanconi syndrome

    B. Cystinosis

  • 78

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Cystine deposits in the cornea

    B. Cystinosis

  • 79

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Inherited disorder of tubular reabsorption

    A. Cystinuria

  • 80

    Place the appropriate letter in front of the following statements. A. Cystinuria B. Cystinosis Early renal calculi formation

    A. Cystinuria

  • 81

    Blue diaper syndrome is associated with: A. Lesch-Nyhan syndrome B. Phenylketonuria C. Cystinuria D. Hartnup disease

    D. Hartnup disease

  • 82

    Homocystinuria is caused by failure to metabolize: A. Lysine B. Methionine C. Arginine D. Cystine

    B. Methionine

  • 83

    The Ehrlich reaction will only detect the presence of: A. Uroporphyrin B. Porphobilinogen C. Coproporphyrin D. Protoporphyrin

    B. Porphobilinogen

  • 84

    Acetyl acetone is added to the urine before performing the Ehrlich test when checking for: A. Aminolevulinic acid B. Porphobilinogen C. Uroporphyrin D. Coproporphyrin

    B. Porphobilinogen

  • 85

    The classic urine color associated with porphyria is: A. Dark yellow B. Indigo blue C. Pink D. Port wine

    D. Port wine

  • 86

    Which of the following specimens can be used for porphyrin testing? A. Urine B. Blood C. Feces D. All of the above

    D. All of the above

  • 87

    The two stages of heme formation affected by lead poisoning are: A. Porphobilinogen and uroporphyrin B. Aminolevulinic acid and porphobilinogen C. Coproporphyrin and protoporphyrin D. Aminolevulinic acid and protoporphyrin

    D. Aminolevulinic acid and protoporphyrin

  • 88

    Hurler, Hunter, and Sanfilippo syndromes are hereditary disorders affecting metabolism of: A. Porphyrins B. Purines C. Mucopolysaccharides D. Tryptophan

    C. Mucopolysaccharides

  • 89

    Many uric acid crystals in a pediatric urine specimen may indicate: A. Hurler syndrome B. Lesch-Nyhan disease C. Melituria D. Sanfilippo syndrome

    B. Lesch-Nyhan disease

  • 90

    Deficiency of the GALT enzyme will produce a: A. Positive Clinitest B. Glycosuria C. Galactosemia D. Both A and C

    D. Both A and C

  • 91

    Match the metabolic urine disorders with their classic urine abnormalities. 1. Cystinuria 2. PKU 3. Indicanuria 4. Alkaptonuria 5. Lesch-Nyhan disease 6. Isovaleric academia A. Sulfur odor B. Sweaty feet odor C. Orange sand in diaper D. Mousy odor E. Black color F. Blue color

    _A_ _D_ _F_ _E_ _C_ _B_

  • 92

    The functions of the CSF include all of the following except: A. Removing metabolic wastes B. Producing an ultrafiltrate of plasma C. Supplying nutrients to the CNS D. Protecting the brain and spinal cord

    B. Producing an ultrafiltrate of plasma

  • 93

    The CSF flows through the: A. Choroid plexus B. Pia mater C. Arachnoid space D. Dura mater

    C. Arachnoid space

  • 94

    Substances present in the CSF are controlled by the: A. Arachnoid granulations B. Blood–brain barrier C. Presence of one-way valves D. Blood–CSF barrier

    B. Blood–brain barrier

  • 95

    What department is the CSF tube labeled 3 routinely sent to? A. Hematology B. Chemistry C. Microbiology D. Serology

    A. Hematology

  • 96

    The CSF tube that should be kept at room temperature is: A. Tube 1 B. Tube 2 C. Tube 3 D. Tube 4

    B. Tube 2

  • 97

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Even distribution of blood in all tubes

    B. Intracranial hemorrhage

  • 98

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Xanthochromic supernatant

    B. Intracranial hemorrhage

  • 99

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Concentration of blood in tube 1 is greater than in tube 3

    A. Traumatic tap

  • 100

    Place the appropriate letter in front of the statement that best describes CSF specimens in these two conditions: A. Traumatic tap B. Intracranial hemorrhage Specimen contains clots

    A. Traumatic tap