Vohwinkel syndrome: ichthyosiform variant in a family
نویسندگان
چکیده
منابع مشابه
Vohwinkel syndrome, ichthyosiform variant - by Camisa - Case report*
Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar keratosis, which manifests in infants and becomes more evident in adulthood. Its mode of inheritance is autosomal dominant with mutation in loricrin and Connexin 26 genes. Patients with this mutation present hyperkeratosis of the palms and soles, constricting bands of the digits, usually on the fift...
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ژورنال
عنوان ژورنال: Anais Brasileiros de Dermatologia
سال: 2018
ISSN: 1806-4841,0365-0596
DOI: 10.1590/abd1806-4841.20187440