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对13三体综合征8例病例中发现的解剖学缺陷和变异谱的检查。

An examination of the spectrum of anatomic defects and variations found in eight cases of trisomy 13.

作者信息

Pettersen J C, Koltis G G, White M J

出版信息

Am J Med Genet. 1979;3(2):183-210. doi: 10.1002/ajmg.1320030209.

Abstract

We report the anatomic variations found in four additional cases of trisomy 13. Data from these and four previous cases [Colacino and Pettersen, 1978] are utilized to define a muscle phenotype. Previously unreported defects include the bilateral presence of cervical ribs and the bilateral absence of 12th thoracic ribs in five of the eight cases. One unusual developmental defect of the great vessels is also described. The findings suggest that a definitive diagnosis of trisomy 13 can be made on the basis of six muscle variations.

摘要

我们报告了另外4例13三体综合征患者中发现的解剖变异情况。利用这些病例以及之前4例病例(Colacino和Pettersen,1978年)的数据来定义一种肌肉表型。之前未报告的缺陷包括8例中有5例双侧存在颈肋以及双侧缺如第12对胸肋。还描述了一种大血管的罕见发育缺陷。这些发现表明,基于六种肌肉变异情况可对13三体综合征作出明确诊断。

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