Autosomal dominant polycystic kidney disease

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Autosomal dominant polycystic kidney disease

Synonyms: ADPKD

A rare genetic renal tubular disease characterized by progressive outgrowths of fluid-filled cysts from the renal epithelium which can manifest with hematuria urinary tract infections hypertension and abdominal or flank pain. The slowly progressive loss of kidney function may evolve to end stage kidney disease (ESKD).

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: // Data version October 2023.

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Autosomal dominant polycystic kidney disease?

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