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关节脱位和脑畸形与IV型口面指综合征始终相关。

Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IV.

作者信息

Digilio M C, Giannotti A, Pagnotta G, Mingarelli R, Dallapiccola B

机构信息

Department of Medical Genetics, Bambino Gesu' Hospital, Rome, Italy.

出版信息

Clin Genet. 1995 Sep;48(3):156-9. doi: 10.1111/j.1399-0004.1995.tb04077.x.

Abstract

We present a female patient with the oral-facial-digital syndrome type IV. Our report, the tenth in the literature, describes the typical manifestations of the syndrome, combined with malformations and deformations which have not always been described in the previously reported cases. They include cerebral and renal anomalies, anal atresia and dislocation of elbows and knees.

摘要

我们报告了一名患有IV型口面指综合征的女性患者。我们的报告是该综合征文献中的第十例,描述了该综合征的典型表现,并伴有先前报道病例中并不总是出现的畸形和变形。这些包括脑和肾异常、肛门闭锁以及肘和膝关节脱位。

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