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因45,X、0/46 双着丝粒(X)嵌合体所致的卵巢发育不全。

Ovarian dysgenesis due to 45 X, 0/46 dic (X) mosaicism.

作者信息

Valenta L J, Higgins J V, Holzman G B

出版信息

J Clin Endocrinol Metab. 1977 Oct;45(4):702-6. doi: 10.1210/jcem-45-4-702.

Abstract

A 16 year old girl was evaluated for short stature, primary amenorrhea, and lack of development of secondary sex characterisics. She did not have the classical phenotypic signs of Turner's syndrome. However, she was short, had infantile genitalia and the adnexa were not palpable. There was a minor bone malformation and no signs of visceral abnormalities. The hormonal studies showed hypergonadotropic hypogonadism and borderline hypothyroidism. The rest of the endocrine functions was normal. The Barr bodies on the buccal smear were decreased and in part abnormal, large or bipartite. The karyotype showed mosaicism of about equal proportions of 45 X, 0/46, X, dic (X). The large dicentric chromosome was due to the end to end fusion of two X chromosomes by their short arms. Sequential binding studies were performed and failed to document any loss of genetic material of the dicentric X. It is speculated that the fusion of X chromosomes during an early mitotic division was responsible for the 45 X, U cell line, and that the short stature and gonadal dysgenesis in this patient was due to the presence of the 45 X, 0 line.

摘要

一名16岁女孩因身材矮小、原发性闭经以及第二性征发育不全而接受评估。她没有特纳综合征的典型表型体征。然而,她身材矮小,生殖器呈幼稚型,附件无法触及。存在轻微骨骼畸形,无内脏异常体征。激素研究显示高促性腺激素性性腺功能减退和临界甲状腺功能减退。其余内分泌功能正常。颊黏膜涂片的巴氏小体减少且部分异常、增大或呈双分体。核型显示约等比例的45,X,0/46,X,dic(X)嵌合体。大的双着丝粒染色体是由于两条X染色体短臂端对端融合所致。进行了序列结合研究,但未能证明双着丝粒X染色体有任何遗传物质丢失。据推测,在早期有丝分裂过程中X染色体的融合导致了45,X,0细胞系的出现,而该患者的身材矮小和性腺发育不全是由于45,X,0细胞系的存在。

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