The first reported case of a variant of Mal de Maleda of the Gamborg-Nielsen type in an Egyptian origin patient

• Auteurs principaux: Khalid M. Al-Husain (Auteur), Ahmed A. Al-Thubaiti1 (Auteur), Farah M. Alzahrani (Auteur), Iqbal A. Bukhari (Auteur), Mohammad El-Shawarby (Auteur)
• Format: Livre
• Publié: Our Dermatology Online, 2018-04-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Mal de Meleda is a rare genodermatosis with an autosomal recessive inheritance. Mutations in the SLURP1 gene are the cause of this disease. Clinically, it is characterized by progressive palmoplantar hyperkeratosis exhibiting a transgradiens pattern extending to the dorsal aspects of the hands and f...