polycystic kidney disease

(redirected from Autosomal recessive polycystic kidney disease)
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Related to Autosomal recessive polycystic kidney disease: Autosomal dominant polycystic kidney disease, ADPKD
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  • noun

Synonyms for polycystic kidney disease

kidney disease characterized by enlarged kidneys containing many cysts

References in periodicals archive ?
Morbidity from congenital hepatic fibrosis after renal transplantation for autosomal recessive polycystic kidney disease.
The chief indication for CPLKT is for rare congenital diseases affecting both liver and kidney (such as primary hyperoxaluria type 1 and autosomal recessive polycystic kidney disease with hepatic fibrosis).
Autosomal recessive polycystic kidney disease is a cystic variant of PKD emerging from mutations in the PKHD1 gene.
7) In this study we propose a diagnostic classification in 5 categories of the entities presenting with glomerular cysts (Table 1): type I, PKD presenting as a GCK variant of autosomal recessive polycystic kidney disease (ARPKD)/ADPKD (with or without liver disease); type II, hereditary GCK synonymous with GCKD.
This leads to different congenital bile duct disorders, such as Caroli disease and syndrome, autosomal recessive polycystic kidney disease, autosomal dominant polycystic kidney disease, congenital hepatic fibrosis, and bile duct hamartomas (BDHs, also known as von Meyenburg complexes).
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