5 Cyst Kidney disorders Flashcards
Cystic dilation of collecting ducts
Autosomal recessive polycystic kidney disease
destroy kidney parenchyma
Autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease sxs
flank pain, hematuria, hypertension, urinary infection, progressive renal failure
Autosomal dominant polycystic kidney disease
due to mutation in
Mutation in PKD1 (85% of cases, chromosome 16) or PKD2 (15% of cases, chromosome 4).
Autosomal dominant polycystic kidney disease Death from complications of 2 dzs
chronic kidney disease or hypertension (caused byrenin production).
berry aneurysm
Autosomal dominant polycystic kidney disease
mitral valve prolaps
Autosomal dominant polycystic kidney disease
benign hepatic cysts.
Autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease
tx
ACE inhibitors or ARBs
Cystic dilation of collecting ducts
Autosomal recessive polycystic kidney disease
Associated with congenital hepatic fibrosis
Autosomal recessive polycystic kidney disease
Potter seq can be due to what in which cyst dz.
ologuria in
Autosomal recessive polycystic kidney disease
Autosomal recessive polycystic kidney disease Concerns beyond neonatal period include 3 conditions
systemic hypertension, progressive renal insufficiency, and portal hypertension from congenital hepatic fibrosis.
Inherited disease causing tubulointerstitial fibrosis and progressive renal insufficiency
Medullary cystic disease
inability to concentrate urine
Medullary cystic disease