Autosomal dominant polycystic kidney disease (Q46418): Difference between revisions
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13 August 2026
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Latest revision as of 14:59, 13 August 2026
Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and due to mutations on chromosomes 16 and 4. Non-renal manifestations can include cysts in the liver and less commonly pancreas. Cerebral arterial aneurysms with subarachnoid haemorrhage, and other non-renal vascular abnormalities can also occur.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | GB81 |
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| English | Autosomal dominant polycystic kidney disease |
Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and due to mutations on chromosomes 16 and 4. Non-renal manifestations can include cysts in the liver and less commonly pancreas. Cerebral arterial aneurysms with subarachnoid haemorrhage, and other non-renal vascular abnormalities can also occur. |
Statements
CID11:GB81
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dki-india-GB81
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Concluído
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13 August 2026
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