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[X连锁鱼鳞病的基因缺失]

[Gene deletion of X-linked ichthyosis].

作者信息

Li M

机构信息

Nanjing Railway Medical College.

出版信息

Zhonghua Yi Xue Za Zhi. 1992 Apr;72(4):210-2, 254.

PMID:1327447
Abstract

The characterization of steroid sulfatase (STS) gene mutation from seven X-linked ichthyotic patients was performed by multiple polymerase chain reaction (MPCR) which amplified two specific regions at the 5' and 3' end of STS gene. The results indicated that five out seven patients were found to have entire STS gene deletion. Two other cases and five patients' mothers showed two amplification fragments. So did two cases of dominant ichthyosis vulgaris. It was further ascertained that entire gene deletion is the main mutation of STS locus in Chinese population. MPCR is a rapid and simple method for gene diagnosis of X-linked ichthyosis.

摘要

通过多重聚合酶链反应(MPCR)对7例X连锁鱼鳞病患者的类固醇硫酸酯酶(STS)基因突变进行了鉴定,该反应扩增了STS基因5'和3'端的两个特定区域。结果表明,7例患者中有5例被发现存在整个STS基因缺失。另外2例患者及其5位母亲显示出两个扩增片段。2例寻常型鱼鳞病显性患者也是如此。进一步确定,整个基因缺失是中国人群中STS基因座的主要突变。MPCR是一种快速、简便的X连锁鱼鳞病基因诊断方法。

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