A Rare Case; Focal Acral Hyperkeratosis

Neşe GÖÇER GÜROK, Savaş Öztürk, Ahmet Kılıçarslan
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Abstract

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 inheritance, 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
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罕见病例;局灶性肢端角化过度
局灶性肢端角化过度症(FAH)是一种罕见的遗传性皮肤病。FAH通常在生命的第二或第三个十年中观察到,它是一种掌跖角化病,一种以手掌和脚底异常增生为特征的异质性疾病。虽然它是常染色体显性遗传,但它也可能是散发性的。它也被称为一种罕见的科斯塔的acrokeratoelastidosis (AKE)变种。其病因尚不清楚,也没有有效的治疗方法。在本研究中,我们报告了一例43岁的FAH病例,由于其罕见且经常与AKE混淆
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审稿时长
16 weeks
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