Autosomal recessive polycystic kidney disease (Q98394): Difference between revisions
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A doença renal policística autossômica recessiva (DRPAR) é uma condição hereditária caracterizada por múltiplos cistos afetando os ductos coletores, dando origem a nefromegalia, hipertensão arterial, infecção do trato urinário e doença renal crônica (insuficiência). O envolvimento do fígado (anormalidades biliares, colangite, hipertensão portal) está frequentemente associado ao quadro. | |||
| description / en | description / en | ||
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. | |||
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. |
