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 8 min This content is machine translated Ichthyoses Broad spectrum of genetic cornification disorders Ichthyoses comprise a heterogeneous group of rare hereditary skin disorders whose classification can prove difficult. Accordingly, rapid diagnosis and therapy initiation is a challenge in everyday clinical practice. Experts specialized…
