Birt–Hogg–Dubé syndrome: Difference between revisions
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It is characterized by: | It is characterized by: | ||
* Skin lesions (fibrofolliculoma, trichodiscoma, [[acrochordon]]). | * Skin lesions (fibrofolliculoma, trichodiscoma, [[acrochordon]]). | ||
* Renal tumours, [[chromophobe renal cell | * Renal tumours, [[chromophobe renal cell carcinoma]] most commonly. | ||
** Other tumours seen, e.g. [[renal oncocytoma|oncocytoma]]. | ** Other tumours seen, e.g. [[renal oncocytoma|oncocytoma]]. | ||
* Variable penetrance (autosomal dominant). | * Variable penetrance (autosomal dominant). | ||