Hereditary benign intraepithelial dyskeratosis

A rare genetic disorder with an autosomal dominant pattern of inheritance with variable penetrance. It was initially described among Native Americans belonging to the Haliwa-Saponi tribe of northeastern North Carolina. It is caused by a duplication of chromosomal DNA at 4q35. Clinical signs present in early childhood and include asymptomatic plaques of the epibulbar conjunctivae and oral mucosa. Clinical progression of the plaques to malignancy has not been reported.

Also known as: HBID, Witkop-Von Sallmann disease, hereditary benign corneal intraepithelial dyskeratosis, Dkbi, dyskeratosis, hereditary benign intraepithelial

16 clinical trials for this condition and its sub-types.