A Male fetus is described with multiple congenital abnormalities including craniosynostosis and bilateral radial aplasia. There are many similarities to the case recently reported by Imaizumi and Kuroki2 (Am J Med Genet 41: 162–163). These cases may represent a new syndrome with overlapping features of the Baller-Gerold and Roberts syndromes.
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机译:男性胎儿被描述为多种先天性异常,包括颅缝早闭和双侧桡骨再生障碍。与Imaizumi和Kuroki最近报告的病例有许多相似之处2(Am J Med Genet 41:162-163)。这些病例可能代表一种新的综合征,具有 Baller-Gerold 和 Roberts 综合征的重叠特征。
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