RENAL DISEASE Flashcards
ETIOLOGY:
Cellular proliferation affects the
capillary walls or the glomerular
basement membrane, possibly immune-mediated
MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS
ETIOLOGY:
Marked decrease in renal function resulting from glomerular damage precipitated by other renal disorders
CHRONIC GLOMERULONEPHRITIS
SIGNIFICANT TESTS FOR CHRONIC GLOMERULONEPHRITIS:
BUN, SERUM, CREATININE, eGFR, ELECTROLYTES
ETIOLOGY:
Deposition of IgA on the glomerular membrane resulting from increased levels of serum, IgA
IMMUNOGLOBULIN A NEPHROPATHY (BERGER’S DISEASE)
ETIOLOGY:
Disruption of the shield of negativity and damage to the tightly fitting podocyte barrier resulting in massive loss of protein and lipids
NEPHROTIC SYNDROME
SIGNIFICANT TESTS FOR NEPHROTIC SYNDROME:
Serum albumin, Cholesterol, Triglycerides
ETIOLOGY:
Disruption of the podocytes occurs primarily in children following allergic reactions and immunizations
MINIMAL CHANGE DISEASE (LIPID NEPHROSIS)
ETIOLOGY:
Disruption of podocytes in certain areas of glomeruli associated with heroin and analgesic abuse and AIDS
FOCAL SEGMENTAL GLOMERULOSCLEROSIS
ETIOLOGY:
Damage to renal tubular cells caused by ischemia or toxic agents
ACUTE TUBULAR NECROSIS
ETIOLOGY:
Inherited in association with cystinosis and Hartnup disease of acquired through exposure to toxic agents
FANCONI SYNDROME
ETIOLOGY:
Genetic disorder showing lamellated and thinning glomerular basement membrane
ALPORT’S SYNDROME
ETIOLOGY:
Inherited defect of tubular response to ADH or acquired from medications
NEPHROGENIC DIABETES INSIPIDUS
TYPE OF NEPHROGENIC DIABETES INSIPIDUS:
- Failure of tubules to respond to
antidiuretic hormone (ADH), inherited sex-linked recessive or lithium and amphotericin B
exposure, polycystic kidneys and sickle cell
anemia
NEPHROGENIC
TYPE OF NEPHROGENIC DIABETES INSIPIDUS:
- Failure to produce ADH
NEUROGENIC
ETIOLOGY:
Inherited autosomal recessive trait
Other significant test: Blood Glucose
RENAL GLYCOSURIA