Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary skin disorder · Keratoacanthoma
Familial keratoacanthoma
Multiple familial keratoacanthoma (KA) of Witten and Zak is a rare a rare inherited skin cancer syndrome and is characterized by the coexistence of features characteristic of both multiple KA, Ferguson Smith type and generalized eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Transmission is autosomal dominant.
This condition has no sub-types.