Kindler syndrome: report of two cases.

Abstract excerpt

Kindler syndrome is a rare autosomal recessive genodermatosis characterized by trauma-induced blisters, progressive poikiloderma and varying degrees of photosensitivity. In 2003, loss-of-function mutations were identified in the gene KIND1 mapped to chromosome 20p12.3. In this paper, we report Kindler syndrome in two children born to consanguineous parents presenting acral blistering, photosensitivity,...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Blister
• Share to Child, Preschool
• Share to Epidermolysis Bullosa