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Renal Diseases - Statistics

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General Stats
  • This quiz has been taken 2 times
  • The average score is 1 of 58
Answer Stats
Hint Answer % Correct
Ascending bacterial infection of the bladder Cystitis
50%
Antineutrophilic cytoplasmic autoantibody (ANCA) binds to neutrophils in vascular walls, producing damage to small vessels in the lungs and glomerulus Wegener’s granulomatosis
50%
Unique screening test for MSUD 2,4-DNPH
0%
Substance secreted by the tumor in melanuria that oxidizes melanogen to melanin 5,6-dihydroxyindole
0%
Allergic inflammation of the renal interstitium in response to certain medications Acute interstitial nephritis
0%
Deposition of immune complexes, formed in conjunction with beta-hemolytic group A Streptococcus infection, on the glomerular membranes Acute Poststreptococcal Glomerulonephritis
0%
Infection of the renal tubules and interstitium related to interference of urine flow to the bladder, reflux of urine from the bladder, and untreated cystitis Acute pyelonephritis
0%
Damage to renal tubular cells caused by ischemia or toxic agents Acute tubular necrosis
0%
Genetic disorder showing lamellated and thinning glomerular basement membrane Alport syndrome
0%
Enzyme deficient in MSUD BCKD
0%
FeCl3 tube test color in PKU blue-green
0%
FeCl3 tube test color in Argentaffinoma Blue-green
0%
Unique screening test for Cystinuria Brand’s Modification of Legal’s nitroprusside
0%
Marked decrease in renal function resulting from glomerular damage precipitated by other renal disorders Chronic Glomerulonephritis
0%
Recurrent infection of the renal tubules and interstitium caused by structural abnormalities affecting the flow of urine Chronic pyelonephritis
0%
Mnemonic for the amino acids involved in the defective tubular reabsorption in Cystinuria COLA
0%
Reagent of the unique screening test for Cystinuria Cyanide nitroprusside
0%
Enzyme deficient in Homocystinuria Cystathione B-synthase
0%
Most common cause of End Stage Renal Disease Diabetic Nephropathy
0%
Damage to the glomerular membrane occurs as a result of glomerular membrane thickening and increased deposition of cellular and noncellular material within the glomerular matrix. Diabetic Nephropathy
0%
2nd Unique screening test for Melanuria Ehrlich Test
0%
Color of the unique screening test for Methylmalonic acidemia Emerald green
0%
Inherited in association with cystinosis and Hartnup disease or acquired through exposure to toxic agents Fanconi syndrome
0%
Disruption of podocytes in certain areas of glomeruli associated with heroin and analgesic abuse and with HIV and hepatitis viruses Focal segmental glomerulosclerosis
0%
Enzyme deficient in Type 1 Tyrosinemia/Tyrosyluria Fumarylacetoacetate hydrolase
0%
Attachment of a cytotoxic antibody formed during viral respiratory infections to glomerular and alveolar basement membranes Goodpasture syndrome
0%
FeCl3 tube test color in Melanuria Gray/Black precipitate
0%
Occurs primarily in children after viral respiratory infections; a decrease in platelets disrupts vascular integrity Henoch-Schonlein Purpura
0%
Enzyme deficient in Alkaptonuria Homogentisic acid oxidase
0%
Enzyme deficient in Lesch-Nyhan Disease hypoxanthine guanine phosphoribosyltransferase
0%
Deposition of IgA on the glomerular membrane resulting from increased levels of serum IgA IgA Nephropathy
0%
Confirmatory test for PKU Ion exchange HPLC
0%
Mnemonic for the acidemias involved in Organic Acidemias IPM
0%
Cellular proliferation affecting the capillary walls or the glomerular basement membrane, possibly immune mediated Membranoproliferative Glomerulonephritis
0%
Thickening of the glomerular membrane after IgG immune complex deposition associated with systemic disorders Membranous Glomerulonephritis
0%
Not metabolized in Homocystinuria Methionine
0%
Disruption of the podocytes occurring primarily in children after allergic reactions and immunizations; dysfunction of T-cell immunity Minimal change disease
0%
Inherited defect of tubular response to ADH or acquired from medications Nephrogenic diabetes insipidus (DI)
0%
Unique screening test for Tyrosyluria/Tyrosinemia Nitroso-naphthol
0%
Unique screening test for Argentaffinoma Nitrosonaphthol with nitrous acid
0%
Unique screening test for Indicanuria Obermayer’s test
0%
Color of the unique screening test for Tyrosyluria/Tyrosinemia orange-red
0%
enzyme deficient in phenylketonuria Phenylalanine hydroxylase
0%
Enzyme deficient in Type 3 Tyrosyluria/Tyrosinemia p-hydroxyphenylpyruvic acid dioxygenase
0%
Unique screening test for Methymalonic acidemia p-nitroaniline tes
0%
Deposition of immune complexes from systemic immune disorders on the glomerular membrane Rapidly Progressive Glomerulonephritis
0%
Color of the unique screening test for Melanuria Red
0%
Color of the unique screening test for Cystinuria Red-purple
0%
Color of the unique screening test for Homocystinuria Red-purple
0%
Inherited autosomal recessive trait Renal glucosuria
0%
Unique screening test for Homocystinuria Silver-nitroprusside test
0%
1st Unique screening test for Melanuria Sodium nitroprusside test
0%
FeCl3 tube test color in Alkaptonuria Transient blue
0%
FeCl3 tube test color in Tyrosyluria/Tyrosinemia transient green
0%
Enzyme deficient in Type 2 Tyrosinemia/Tyrosyluria Tyrosine aminotransferase
0%
Inherited defect in the production of normal uromodulin by the renal tubules and increased uric acid causing gout Uromodulin-associated kidney disease
0%
Color of the unique screening test for Indicanuria Violet
0%
Color of the unique screening test for Argentaffinoma Violet
0%
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