This content is machine translated Case Report KID syndrome – a rare ectodermal dysplasia Keratitis-ichthyosis-deafness syndrome (KID) is a very rare genodermatosis. The main symptoms include ichthyosiform scaling of the skin, hyperkeratosis of the palms, sensory deafness and keratitis. Typical complications are severe skin...…
View Post 2 min This content is machine translated Rare skin diseases Clouston syndrome – a hidrotic ectodermal dysplasia. Clouston syndrome is an autosomal dominant inherited disorder characterized by the leading symptoms of hyperkeratosis, nail dystrophy and alopecia. The syndrome is caused by mutations in the GJB6 gene, which…
