Aliases:
Polycystic Kidney Disease, Infantile, Type 1
Polycystic Kidney Disease, Infantile, Type I
Polycystic Kidney and Hepatic Disease 1
ARPCKD

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A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY.
www.nlm.nih.gov/cgi/mesh/...

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Aug 16, 2012
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May have portal hypertension. Consider oesophageal varices, variceal bleeding and porto-systemic shunting.

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Jul 20, 2011
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Avoid NSAIDs if non-anuric ESRD/ESRF or renal transplant

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May 18, 2011
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