bn:01390291n
Noun Concept
Categories: Autosomal recessive disorders, Palmoplantar keratodermas, Genodermatoses, Rare diseases
EN
Mal de Meleda  Meleda disease  Gamborg-Nielsen  Gamborg-Nielsen keratoderma  Gamborg–Nielsen
EN
Meleda disease or "mal de Meleda", also called Mljet disease, keratosis palmoplantaris and transgradiens of Siemens, is an extremely rare autosomal recessive congenital skin disorder in which dry, thick patches of skin develop on the soles of the hands and feet, a condition known as palmoplantar hyperkeratosis. Wikipedia
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EN
Meleda disease or "mal de Meleda", also called Mljet disease, keratosis palmoplantaris and transgradiens of Siemens, is an extremely rare autosomal recessive congenital skin disorder in which dry, thick patches of skin develop on the soles of the hands and feet, a condition known as palmoplantar hyperkeratosis. Wikipedia
Human disease Wikidata
GENETIC ASSOCIATION
HEALTH SPECIALTY