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Crouzon 综合征中纤维母细胞生长因子受体 2 基因 c.1061C>G(p.Ser354Cys)突变导致严重的三叶形颅面骨畸形。

Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon Syndrome.

机构信息

Australian Craniofacial Unit.

Division of Plastic Surgery, Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

J Craniofac Surg. 2021;32(1):261-264. doi: 10.1097/SCS.0000000000006999.

Abstract

Cloverleaf skull deformity (CSD), or Kleeblattschädel, is a condition with severe and unpatterned multisuture craniosynostosis, resulting in a trilobar-shaped skull. This deformity mainly comprises a cranio-orbito-facial malformation that leads to a spectrum of multidisciplinary issues. Several syndromes are associated with CSD, such as Crouzon syndrome (CS). Here, we report the case of an infant with CS and the pathogenic c.1061C>G (p.Ser354Cys) variant of the fibroblast growth factor receptor 2 (FGFR2) gene. The child presented with the severe form of CSD despite having a normal, mid-trimester, sonographic scan.

摘要

三叶形颅骨畸形(CSD),又称克莱布特拉赫特尔畸形,是一种严重且无模式的多缝颅缝早闭症,导致三叶形颅骨。这种畸形主要包括颅面眶畸形,导致一系列多学科问题。几种综合征与 CSD 相关,如克鲁宗综合征(CS)。在这里,我们报告了一例患有 CS 的婴儿,其纤维母细胞生长因子受体 2(FGFR2)基因存在 c.1061C>G(p.Ser354Cys)致病性变异。尽管患儿在中期超声扫描中表现正常,但仍呈现出 CSD 的严重形式。

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