A Rare Case; Focal Acral Hyperkeratosis
Öz
Focal acral hyperkeratosis (FAH) is a rare genodermatosis. FAH is usually observed in the second or third decades of life, and it is a type of palmoplantar
keratoderma, a heterogeneous group of diseases characterized by abnormal incrassation of the palms and soles. Although it is an autosomal dominant inher-
itance, it could also be sporadic. It is also known as a rare variant of Costa’s Acrokeratoelastoidosis (AKE). Its etiology is not known clearly and there is no
effective treatment. In the present study, a 43-year-old recently diagnosed FAH case is presented due to its rarity and frequent confusion with AKE based
on current literature.
Anahtar Kelimeler
Autosomal dominant inheritance, focal acral hyperkeratosis, palmoplantar keratoderma.
Proje Numarası
Yok
Kaynakça
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