Cylindromatosis, familial: See: Familial cylindromatosis.
Familial cylindromatosis: A genetic syndrome in which numerous benign tumors of skin adnexa (such as the sweat glands) develop, principally on the head and neck.
Cylindromatosis, familial symptoms, causes, diagnosis, and treatment information for Cylindromatosis, familial (Familial cylindromatosis) with alternative diagnoses, full ...
A US Department of Health and Human Service project providing information on genetic and rare diseases. A comprehensive body of resources on Familial cylindromatosis
Pathogenic mutations in CYLD can be identified in patients affected with Brooke-Spiegler syndrome, (Familial) Cylindromatosis or multiple familial trichoepithelioma.
Familial cylindromatosis information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.