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最初被诊断为寻常型鱼鳞病或X连锁隐性鱼鳞病患者的类固醇硫酸酯酶缺乏症。

Steroid sulphatase deficiency in patients initially diagnosed as ichthyosis vulgaris or recessive X-linked ichthyosis.

作者信息

Yoshiike T, Matsui T, Ogawa H

出版信息

Br J Dermatol. 1985 Apr;112(4):431-3. doi: 10.1111/j.1365-2133.1985.tb02316.x.

Abstract

Twenty-one patients with ichthyosis were classified as either ichthyosis vulgaris (IV) (five cases) or recessive X-linked ichthyosis (RXLI) (sixteen cases) by using a steroid sulphatase assay of plantar callus and peripheral leukocytes. The patients had presented with various clinical manifestations, which had resulted in some initial misdiagnoses. Cases which initially resemble IV may in fact be RXLI, although we found that if a case is initially diagnosed as RXLI it is unlikely to be a case of IV.

摘要

通过对足底胼胝和外周血白细胞进行类固醇硫酸酯酶检测,将21例鱼鳞病患者分为寻常型鱼鳞病(IV)(5例)或隐性X连锁鱼鳞病(RXLI)(16例)。这些患者表现出各种临床表现,导致了一些最初的误诊。最初类似IV的病例实际上可能是RXLI,尽管我们发现如果一个病例最初被诊断为RXLI,那么它不太可能是IV。

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