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9例Y染色体长臂分子定义性缺失男性患者的临床特征

Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm.

作者信息

Salo P, Ignatius J, Simola K O, Tahvanainen E, Kääriäinen H

机构信息

Department of Medical Genetics, University of Helsinki, Finland.

出版信息

J Med Genet. 1995 Sep;32(9):711-5. doi: 10.1136/jmg.32.9.711.

Abstract

Deletions of the long arm of the Y chromosome have previously been associated with azoospermia and short stature. We report the results of a detailed clinical and molecular study of nine males with partial deletions of Yq. Special emphasis was laid on congenital anomalies and dysmorphic features. Some of the patients have developmental problems or distinct facial features, namely a small chin and mouth, a high arched or cleft palate, downward slanting palpebral fissures, high nasal bridge, and dysmorphic ears. As far as we know, similar facial dysmorphism has not been previously described in association with del(Yq). These features are not, however, simply correlated to the size of the deletion. In none of these patients could evidence of aberrant Xq-Yq interchange be found.

摘要

Y染色体长臂缺失先前已被证实与无精子症和身材矮小有关。我们报告了对9名Yq部分缺失男性进行的详细临床和分子研究结果。特别关注了先天性异常和畸形特征。部分患者存在发育问题或明显的面部特征,即小下巴、小嘴、高拱或腭裂、睑裂向下倾斜、鼻梁高以及耳部畸形。据我们所知,此前尚未有与del(Yq)相关的类似面部畸形的描述。然而,这些特征并非简单地与缺失大小相关。在这些患者中均未发现异常Xq-Yq互换的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b375/1051672/bc96e4b4145b/jmedgene00276-0043-a.jpg

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