首页> 外文期刊>American journal of medical genetics, Part A >An Infant with Large Fontanelles, Aplasia Cutis Congenita, Tessier Facial Cleft, Polydactyly Inversus, and Toe Syndactyly: A Previously Undescribed Syndrome?
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An Infant with Large Fontanelles, Aplasia Cutis Congenita, Tessier Facial Cleft, Polydactyly Inversus, and Toe Syndactyly: A Previously Undescribed Syndrome?

机译:有大Font门,先天性发育不良,Tessier面部裂痕,多指反位和趾趾的婴儿:以前没有描述过的综合征吗?

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摘要

We report on a 5-month-old female with large and widely spaced anterior and posterior fontanelles, aplasia cutis congenita, Tessier 3 oblique facial cleft, polydactyly, and syndactyly of toes. The polydactyly is unusual as an accessory finger is attached to the left fifth finger with mirrored, end-to-end fusion. We are naming this anomaly polydactyly inversus. The infant appears to have a previously unreported syndrome of unknown cause. (c) 2015 Wiley Periodicals, Inc.
机译:我们报告了一个5个月大的女性,其前font和后font大而隔开,先天性角膜发育不全,Tessier 3斜面部裂口,多指和趾间趾。多指畸形是不寻常的,因为辅助手指通过镜像的端到端融合连接到左手第五个手指。我们将这个异常命名为多态。婴儿似乎患有先前未报告的原因未知的综合症。 (c)2015年威利期刊有限公司

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