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具有45,X染色体组成的特纳综合征患者的妊娠情况。

Pregnancy in the Turner syndrome with only 45,X chromosomal constitution.

作者信息

Wray H L, Freeman M V, Ming P M

出版信息

Fertil Steril. 1981 May;35(5):509-14.

PMID:7227566
Abstract

A 31-year-old white female, 127 cm tall and with other findings of the Turner syndrome, had had normal menses and had become pregnant at ages 23 and 26 years. Chromosomal analyses of several tissues, including both ovaries, revealed only 45,X karyotypes. Both of her daughters had 46,XX karyotypes in lymphocytes. This patient and nine other reported cases of fertile, apparently nonmosaic 45,X women illustrate an extreme of ovarian function in the Turner syndrome and raise questions about the absolute need for XX oocytes in ovarian development. The possibility of pregnancy must be considered in all patients with Turner syndrome, a relatively common chromosomal disorder.

摘要

一名31岁的白人女性,身高127厘米,有特纳综合征的其他表现,月经正常,曾在23岁和26岁时怀孕。对包括双侧卵巢在内的多个组织进行染色体分析,结果显示核型均为45,X。她的两个女儿淋巴细胞的核型均为46,XX。该患者以及其他9例已报道的可育、明显非嵌合型45,X女性病例,展现了特纳综合征中卵巢功能的一个极端情况,并引发了关于卵巢发育中XX卵母细胞是否绝对必需的疑问。对于所有特纳综合征患者(一种相对常见的染色体疾病),都必须考虑其怀孕的可能性。

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