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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Synonyms for polycystic kidney disease

kidney disease characterized by enlarged kidneys containing many cysts

References in periodicals archive ?
Autosomal recessive polycystic kidney disease is the most common heritable cystic renal disease with mutations of a single localized gene in an area in Chromosome 6 (PHKD1).
Autosomal recessive polycystic kidney disease diagnosed in fetus: Indian J Urol 2007; 23:328-9.
Proximal tubular cysts in fetal human autosomal recessive polycystic kidney disease.
Correlation of Kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.
New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications.
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein.
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).
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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