Autosomal recessive polycystic kidney disease (Q98394): Difference between revisions
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15 August 2026
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Latest revision as of 14:50, 16 August 2026
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited condition characterised by multiple cysts affecting the collecting ducts giving rise to nephromegaly, arterial hypertension, urinary tract infection and chronic kidney disease (failure). Liver involvement (biliary abnormalities, cholangitis, portal hypertension) are frequently associated.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1424110943 |
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| English | Autosomal recessive polycystic kidney disease |
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited condition characterised by multiple cysts affecting the collecting ducts giving rise to nephromegaly, arterial hypertension, urinary tract infection and chronic kidney disease (failure). Liver involvement (biliary abnormalities, cholangitis, portal hypertension) are frequently associated. |
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CID11:ID_1424110943
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dki-india-ID_1424110943
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Concluído
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15 August 2026
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