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Superficial Epidermolytic Ichthyosis-Hypertrichosis as a Clue to Diagnosis

机译:表浅表皮溶解性鱼鳞病-肥大症为诊断线索

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摘要

Superficial epidermolytic ichthyosis (SEI) is an autosomal dominant disorder caused by a mutation in the keratin 2 gene and clinically characterized by mild hyperkeratosis, superficial blisters and shedding, referred to as the moulting phenomenon. We report a case of SEI in an 18-month-old girl presenting with marked hypertrichosis. Although not invariably present, we believe that hypertrichosis can be an important clue for diagnosis.
机译:浅表性表皮鱼鳞病(SEI)是由角蛋白2基因突变引起的常染色体显性遗传疾病,临床上以轻度角化过度,浅水泡和脱落为特征,被称为蜕皮现象。我们报告了一名18岁大女孩的SEI病例,该女孩表现出明显的过度毛发。尽管并非总是存在,但我们认为肥大症可能是诊断的重要线索。

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