Autosomal dominant polycystic kidney disease (Q46418): Difference between revisions

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Cistos múltiplos em ambos os rins aumentando em número e tamanho a partir da adolescência, associados ao desenvolvimento de hipertensão e insuficiência renal crônica. O padrão familiar autossômico dominante é comum e devido a mutações nos cromossomos 16 e 4. As manifestações não renais podem incluir cistos no fígado e menos comumente no pâncreas. Aneurismas arteriais cerebrais com hemorragia subaracnoide e outras anormalidades vasculares não renais também podem ocorrer.
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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.

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.
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    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.

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