Dermatoosteolysis, Kirghizian type

Dermatoosteolysis, Kirghizian type, is characterized by recurrent skin ulceration, arthralgia, fever, peri-articular osteolysis, oligodontia and nail dystrophy. This disease has been described in five sibs in a family of Kirghizian origin (Central Asia). Three of the sibs also presented with keratitis leading to visual impairment or blindess. Transmission is autosomal recessive.

Also known as: dermatoosteolysis, Kirghizian type, Dermatoosteolysis Kirghizian type, Kirghizian Dermatoosteolysis, autosomal recessive syndrome of skin ulceration, arthroosteolysis with pseudoacromegaly, keratitis, and oligodontia

0 clinical trials for this condition and its sub-types, 0 tagged with Dermatoosteolysis, Kirghizian type itself.