Braun-Falco O, Schurig V, Meurer M, Klepzig K
Hautarzt. 1985 Mar;36(3):132-41.
We report on a keratinization disorder in four brothers in a family in which members had been affected in three generations. Clinical signs and genetic, histopathologic, autoradiographic and ultrastructural examinations all support the diagnosis of hystrixlike, proliferative ichthyosis with cornoid lamellae and autosomal dominant inheritance. The relationship of the disorder to other hystrixlike genetic keratinization disorders is discussed.
我们报告了一个家族中四名兄弟患有的一种角化异常疾病，该家族三代成员均受此影响。临床体征以及基因、组织病理学、放射自显影和超微结构检查均支持诊断为带有角样板层的豪猪状、增殖性鱼鳞病，且为常染色体显性遗传。本文还讨论了该疾病与其他豪猪状遗传性角化异常疾病的关系。
