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[特纳综合征。165例特纳综合征患者的细胞遗传学分析。首次报告]

[Turner syndrome. Cytogenetic analysis of 165 patients with Turner syndrome. 1st report].

作者信息

Vignetti P, Brinchi V, Bruni L, Rizzuti A, Tarani L, Tozzi M C

机构信息

Cattedra di Clinica Pediatrica, Università La Sapienza, Roma.

出版信息

Minerva Pediatr. 1990 Jan-Feb;42(1-2):25-7.

PMID:2336052
Abstract

Results are reported of a cytogenetic study on 165 patients with Turner syndrome, based on sex chromatin and karyotype tests. We found that the karyotype 45,X is present only in 54.54% of the cases in homogeneous form and in about 14% of the cases in mosaic form associated with a normal clone 46,XX or, rarely, also with a clone 47,XXX; in the other cases X structural anomalies and different kinds of mosaic forms are present. We also found 5 pregnancies in 2 patients: only 2 daughters were born and alive, the first was normal and the second presented the same karyotype and clinical picture of her mother.

摘要

报告了一项基于性染色质和核型检测对165例特纳综合征患者进行的细胞遗传学研究结果。我们发现,核型45,X仅以纯合形式存在于54.54%的病例中,以嵌合形式存在于约14%的病例中,与正常克隆46,XX相关,或很少与克隆47,XXX相关;在其他病例中存在X结构异常和不同类型的嵌合形式。我们还在2例患者中发现了5次妊娠:仅2名女儿出生且存活,第一个正常,第二个具有与其母亲相同的核型和临床表现。

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