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一名患有II型耳-腭-指综合征的男孩及其母亲的扩展表型。

Extended phenotypes in a boy and his mother with oto-palato-digital-syndrome type II.

作者信息

Kaissi Ali Al, Kraschl Raimund, Kaulfersch Wilhelm, Grill Franz, Ganger Rudolf

机构信息

First Medical Department, Ludwig Boltzmann Institute of Osteology, at the Hanusch Hospital of WGKK and, AUVA Trauma Centre Meidling, Hanusch Hospital Vienna, Austria ; Paediatric Department, Orthopaedic Hospital of Speising Vienna, Austria.

Department of Pediatric and Neonatology, Klagenfurt Clinic Klagenfurt, Austria.

出版信息

Clin Case Rep. 2015 Sep;3(9):762-6. doi: 10.1002/ccr3.317. Epub 2015 Aug 20.

Abstract

We describe additional phenotypic features in a boy and his mother. Both manifested the phenotypic/genotypic correlation of oto-palato-digital syndrome type II. The mother's radiographs showed wormian bones of the skull, and paranasal bossing, her feet showed bilateral fusion of the cuboid with the lateral cuneiform bone with subsequent development of metatarsus varus associated with dysplastic distal phalanges.

摘要

我们描述了一名男孩及其母亲的其他表型特征。两人均表现出II型耳-腭-指综合征的表型/基因型相关性。母亲的X光片显示颅骨有缝间骨和鼻旁隆突,她的足部显示骰骨与外侧楔骨双侧融合,随后出现内翻足,并伴有发育不良的远端指骨。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e75/4574794/5400e7aef71b/ccr30003-0762-f1.jpg

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