Loricrin keratoderma

A diffuse palmoplantar keratoderma, characterized by honeycomb palmoplantar hyperkeratosis associated with pseudoainhum of the fifth digit of the hand, ichthyosis and deafness. Keratoderma hereditarium mutilans with ichthyosis follows an autosomal dominant mode of transmission.

Also known as: Camisa disease, Vohwinkel syndrome with ichthyosis, keratoderma hereditarium mutilans with ichthyosis, keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome, loricrin keratoderma, Vohwinkel syndrome, variant form, mutilating keratoderma with ichthyosis

0 clinical trials for this condition and its sub-types, 0 tagged with Loricrin keratoderma itself.