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X连锁隐性鱼鳞病。对一个于1928年首次描述的家族进行重新研究。

X-linked recessive ichthyosis. Reinvestigation of a family first described in 1928.

作者信息

Schlammadinger J, Meyer J C, Vajda I, Szabó G

机构信息

Institute of Biology, University Medical School, Debrecen, Hungary.

出版信息

Dermatologica. 1987;175(5):217-23.

PMID:3479355
Abstract

Recent findings in a family with X-linked recessive ichthyosis are presented. The first description of this family in the literature was given and correctly diagnosed by Csörsz in 1928. His paper can be considered one of the most widely cited proofs of the existence of X-linked ichthyosis. The extended pedigree as well as data of steroid sulfatase and arylsulfatase C determinations presented in this paper verify the diagnosis of the X-linked mode of inheritance of ichthyosis in this family. The biochemical investigations carried out on leukocytes of family members resulted not only in a confirmation of the clinico-genetic diagnosis, but they also helped to establish the heterozygous genotype of a female mentioned previously as an affected person.

摘要

本文介绍了一个患有X连锁隐性鱼鳞病的家族的最新研究结果。该家族在文献中的首次描述由Csörsz于1928年给出并得到正确诊断。他的论文可被视为X连锁鱼鳞病存在的最广泛引用的证据之一。本文展示的扩展谱系以及类固醇硫酸酯酶和芳基硫酸酯酶C测定数据证实了该家族鱼鳞病的X连锁遗传模式诊断。对家族成员白细胞进行的生化研究不仅证实了临床遗传诊断,还帮助确定了之前被提及为患病个体的一名女性的杂合基因型。

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