Beckwith-Wiedemann 综合征
基因病名称(英)
Beckwith-Wiedemann syndrome
基因病名称
Beckwith-Wiedemann 综合征
别名(英)
EMG syndrome,Exomphalos-macroglossia-gigantism syndrome
统计
reviewed:2; annotated:0
交叉引用
130650,C0004903,D001506
描述(英)
A disorder characterized by anterior abdominal wall defects including exomphalos (omphalocele), pre- and postnatal overgrowth, and macroglossia. Additional less frequent complications include specific developmental defects and a predisposition to embryonal tumors.
描述
一种以前腹壁缺陷为特征的疾病，包括脐膨出（脐膨出）、产前和产后过度生长以及巨舌症。其他不太常见的并发症包括特定的发育缺陷和胚胎肿瘤的易感性。