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

• मुख्य लेखकों: Khalid M. Al-Husain (लेखक), Ahmed A. Al-Thubaiti1 (लेखक), Farah M. Alzahrani (लेखक), Iqbal A. Bukhari (लेखक), Mohammad El-Shawarby (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Our Dermatology Online, 2018-04-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...