Exam 1 Flashcards
two dominant manifestations of acute glomerulonephritis
Proteinuria and hematuria
causes of acute glomerulonephritis
immune complex disease, hereditary, metabolic disorder
clinical manifestations of acute tubular necrosis
decreased urine flow, inability to concentrate urine, and loss of many tubular epithelial cells into urine
what is acute tubular necrosis associated with
reduced blood supply to renal tubules
three manifestations of nephrotic syndrome
proteinuria, hypoproteinemia, and edema
common causes of urinary obstruction
congenital malformation, stricture from infection, tumors, and calculi
explain pyelonephritis
infection of kidney and renal pelvis which initially affects renal interstitial but progresses into renal tubules
two main clinical findings in urine that may indicate diabetes mellitus
glycosuria and ketonuria
what would you expect to see in regards to volume and SG in diabetes mellitus
increased SG and increased volume
what is unconjugated bilirubin
linked loosely to albumin, insoluble in water so not found in urine
what is conjugated bilirubin
unconjugated bilirubin that has been conjugated by esterification by glucuronic acid in the liver, now water soluble
what is urobilinogen
conjugated bilirubin that is reduced by the intestinal flora of the small intestine
What is PKU
patient lacks phenylalanine hydroxylase for the conversion of phenylalanine to tyrosine
how would PKU be detected
the metabolite phenylpyruvic acid appears in the urine; diagnosed by phentest which uses ferric ions: dk green to blue green
what is alkaptonuria
patient lacks homogentistic acid oxidase
how is alkaptonuria detected
homogentistic acid accumulates in the blood, body fluids, and urine; gives orange color with Clinitest tablet
what is maple syrup disease
patient lacks enzyme needed in branched-chain amino acid metabolism
how is maple syrup disease detected
accumulation of leucine, isoleucine, keto, and hydroxy acid in urine, blood, and CSF; maple syrup odor; gives purple color with Acetest tablet
what is Fanconi’s syndrome
the proximal convoluted tubule function of the kidney is impaired
how is Fanconi’s syndrome detected
produces a deficiency of blood phosphates, aminoaciduria, and glycosuria
what is cystinuria
urinary excretion of large amounts of the amino acid cystine, as well as arginine, lysine, and ornithine
how is cystinuria detected
cystine calculi are produced due to the ability of cystine to readily precipitate in acid pH
what is galactosemia
patient is able to break down lactose to glucose and galactose, but lack the enzyme to convert galactose to glucose causing galactose to accumulate
how is galactosemia detected
detected in infancy as diarrhea, vomiting, and failure to thrive; neg on dipstick and pos on Clinitest