The cerebro-costo-mandibular syndrome: seven patients and review of the literature

被引:20
作者
van den Ende, JJ
Schrander-Stumpel, C
Rupprecht, E
Meinecke, P
Maroteaux, P
de Die-Smulders, C
Hamel, BCJ
机构
[1] Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[2] Maastricht Univ, Div Clin Genet, Maastricht, Netherlands
[3] Tech Univ Dresden, Klin Kinderheilkunde, Div Radiol, Dresden, Germany
[4] Altonaer Kinderkrankenhaus, Div Human Genet, Hamburg, Germany
[5] Hop Necker Enfants Malad, Div Clin Genet, Paris, France
关键词
Pierre-Robin sequence; posterior rib defects; genetic heterogeneity; cerebro-costo-mandibular syndrome;
D O I
10.1097/00019605-199804000-00002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report seven patients with the cerebro-costo-mandibular syndrome, a multiple congenital anomaly syndrome with, as the most distinctive features extreme micrognathia and abnormal rib development. Twice a parent to child transmission was found, compatible with autosomal dominant mode of inheritance. One of our patients presented with absence of the auditory canals and subluxation of the radial head, and another with choanal atresia, findings that have not been published previously. Longterm follow-up of some of the patients is described, and an overview of the literature is given. (C) Chapman & Hall Ltd.
引用
收藏
页码:87 / 95
页数:9
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