Disease of the island of Meleda or keratoderma of Meleda
نویسندگان
چکیده
منابع مشابه
[Meleda disease (Mal de Meleda): historical shifts in perception].
Nowadays, hereditary diseases are viewed through molecular mechanisms, and one of them, which keeps occurring rather frequently in medical publications, has been named after the Island of Mljet. The world first learned about mal de Meleda from a Dubrovnik physician Luka Stulli in 1826. He described it in a number of his island patients as a non-contagious hereditary skin disease, and named it m...
متن کاملA Case Report of Transgrediant Palmoplantar Keratoderma (Mal de Meleda)
Mal de Meleda is a rare autosomal recessive transgredient keratoderma .Onset is in early childhood, and the development of hyperkeratosis is preceded by erythema. Patches of waxy ivory-yellow hyperkeratosis extend across the whole palms and soles, and on to the dorsal surfaces of hands and feet. Similar lesions of knees and elbows may develop. We describe an 18 year old man with the diagnosis o...
متن کاملKeratoderma Palmoplantaris Transgrediens (Mal de Meleda): A case report
Mal de meleda (Keratoderma plamoplantaris transgrediens) is a rare autosomal recessive form of palmoplantar keratoderma with hyperkeratosis of palms and soles, which appears soon after birth and progressively involves other areas (Transgrediens) of the skin especially dorsal aspects of hands and feet. We report a 20-year-old woman with mal de meleda with some unusual clinical features, i....
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چکیده ندارد.
15 صفحه اولMal de meleda - through history and today.
Meleda disease is an indigenous dermatological disease classified as a hereditary palmoplantar keratoderma. The disease was first described on the island of Mljet, Croatia, by Luko Stulli in 1826. We present a historical review of the literature data throughout the centuries till today. Recently, the gene responsible for the disease has been identified on chromosome 8qter within the cluster of ...
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ژورنال
عنوان ژورنال: Vestnik dermatologii i venerologii
سال: 2020
ISSN: 2313-6294,0042-4609
DOI: 10.25208/vdv518-2020-96-4-67-71