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1例法伊弗综合征病例。

A case of Pfeiffer syndrome.

作者信息

Park Moon Sung, Yoo Jae Eon, Chung Jaiho, Yoon Soo Han

机构信息

Department of Pediatrics, Ajou University School of Medicine, Yongtong-gu, Suwon, Korea.

出版信息

J Korean Med Sci. 2006 Apr;21(2):374-8. doi: 10.3346/jkms.2006.21.2.374.

Abstract

Pfeiffer Syndrome is as rare as Apert syndrome in the Western population. This condition is very rare in the Asian population and has not been previously reported in Korea. The authors report with a review of literature the case of a newborn baby with Pfeiffer syndrome, manifested by bicoronal craniosynostosis, broad thumbs, and big toes. The infant also had bilateral syndactyly of the fingers and toes, mild proptosis, choanal hypoplasia and maxillary hypoplasia.

摘要

在西方人群中,法伊弗综合征与阿佩尔综合征一样罕见。这种病症在亚洲人群中极为罕见,此前在韩国尚无相关报道。作者通过文献回顾报告了一例患有法伊弗综合征的新生儿病例,其表现为双冠状缝早闭、拇指宽大和脚趾粗大。该婴儿还患有手指和脚趾双侧并指(趾)畸形、轻度眼球突出、后鼻孔发育不全和上颌骨发育不全。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a84/2734025/009f08fbdfb0/jkms-21-374-g001.jpg

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