Mental retardation, robin sequence, and brachydactyly: Further confirmation of a new syndrome

被引:1
|
作者
Gurrieri, F
Scarano, G
Garavelli, L
Della Monica, M
Lonardo, F
Cuda, D
Banchini, G
Opitz, JM
Neri, G
机构
[1] Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med, I-00168 Rome, Italy
[2] Azienda Osped G Rummo, UO Genet Med, Benevento, Italy
[3] Arcispedale S Maria Nuova, Ambulatorio Genet Clin Div Pediat, Reggio Emilia, Italy
[4] Arcispedale S Maria Nuova, UO Otorinolaringoiatria, Reggio Emilia, Italy
[5] Arcispedale S Maria Nuova, Dipartimento Materno Infantile, Reggio Emilia, Italy
[6] Univ Utah, Div Med Genet, Dept Pediat, Salt Lake City, UT USA
关键词
new MCA/MR syndrome; cleft soft palate; short digits; Robin sequence;
D O I
10.1002/ajmg.a.20575
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recently we reported two sibs, brother and sister, with a new multiple congenital anomalies/mental retardation (MCA/MR) syndrome characterized by mild to moderate psychomotor delay, Robin sequence, distinctive facial appearance, and brachydactyly. We have subsequently observed a similar pattern of anomalies in two unrelated patients who also showed additional clinical findings. This new observation supports the existence of a new syndrome and expands the phenotypic spectrum of the condition. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:204 / 207
页数:4
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