Elliott A M, Meagher-Villemure K, Oudjhane K, der Kaloustian V M
F. Clarke Fraser Clinical Genetics Unit, Division of Medical Genetics, Montreal Children's Hospital, Quebec, Canada.
Clin Dysmorphol. 1996 Apr;5(2):135-42. doi: 10.1097/00019605-199604000-00005.
We describe a male infant with findings typical of Schinzel-Giedion syndrome. Characteristic features include: midface retraction, widely patent fontanelles, hirsutism, choanal stenosis, hypospadias with chordae, club feet and broad ribs. The patient suffered from seizures and died at 14 months of age of fulminant bronchopneumonia. Pathological examination revealed steatosis in the liver as well as lipid vacuolization of the zona fasciculata of the adrenals.
我们描述了一名患有典型辛泽尔-吉迪恩综合征的男婴。特征性表现包括:面中部凹陷、囟门广泛开放、多毛症、后鼻孔狭窄、伴有系带的尿道下裂、马蹄内翻足和肋骨增宽。该患者患有癫痫发作,14个月时死于暴发性支气管肺炎。病理检查显示肝脏脂肪变性以及肾上腺束状带脂质空泡形成。