Eun So-Hee, Ha Ki Ssu, Je Bo-Kyung, Lee Eung Seok, Choi Byung Min, Lee Jung Hwa, Eun Baik-Lin, Yoo Kee Hwan
Department of Pediatrics, College of Medicine, Korea University, Seoul, Korea.
J Korean Med Sci. 2007 Apr;22(2):352-6. doi: 10.3346/jkms.2007.22.2.352.
Here we report the first case of a Korean infant with a cloverleaf-shaped craniosynostosis, in which the diagnosis of Beare-Stevenson syndrome was suspected upon observation of the typical morphological features. This infant exhibited craniofacial anomalies, ocular proptosis, cutis gyrata, acanthosis nigricans, prominent umbilical stump, furrowed palms and soles, hypospadia, and sacral skin tag coupled with dermal sinus tract. Brain magnetic resonance imaging revealed that the patient also had non-communicating hydrocephalus with Chiari malformation. This is the 8th report of Beare-Stevenson syndrome in the literature, which was confirmed by the detection of a Tyr375Cys mutation in the fibroblast growth factor receptor 2 (FGFR2) gene.
在此,我们报告首例患有三叶草形颅缝早闭的韩国婴儿病例,根据典型形态特征观察怀疑其患有贝亚 - 史蒂文森综合征。该婴儿表现出颅面畸形、眼球突出、皮肤松垂症、黑棘皮病、脐残端突出、手掌和足底有沟纹、尿道下裂以及骶尾部皮肤赘生物伴皮窦道。脑部磁共振成像显示该患者还患有非交通性脑积水合并Chiari畸形。这是文献中关于贝亚 - 史蒂文森综合征的第8例报告,通过检测成纤维细胞生长因子受体2(FGFR2)基因中的Tyr375Cys突变得以确诊。