Brodin M B, Porter P S
Cutis. 1980 Aug;26(2):185-8, 191.
A case of Netherton's syndrome is reported herein and twenty-four previous cases reviewed and tabulated with respect to age, sex, family history, intelligence, consanguinity, aminoaciduria, atopy, recurrent infections, and IgG. This syndrome is characterized by the presence of trichorrhexis invaginata, a distinctive hair shaft abnormality, and either ichtyosis linearis circumflexa or congenital ichthyosiform erythroderma. Recent investigations have shed light upon the pathogenesis of this disease but the precise structural, biochemical, and genetic abnormalities have not been elucidated.
本文报告1例Netherton综合征病例,并对之前的24例病例进行了回顾,根据年龄、性别、家族史、智力、近亲结婚、氨基酸尿症、特应性、反复感染和免疫球蛋白G进行了列表分析。该综合征的特征是存在套叠性脆发症(一种独特的毛干异常),以及回旋线状鱼鳞病或先天性鱼鳞病样红皮病。最近的研究揭示了这种疾病的发病机制,但确切的结构、生化和基因异常尚未阐明。