Devriendt K, D'Espallier L, Fryns J P
Centre for Human Genetics, University of Leuven, Belgium.
J Med Genet. 1996 Mar;33(3):224-6. doi: 10.1136/jmg.33.3.224.
We present a child with severe mental retardation, a central nervous system malformation, signs of ectodermal dysplasia, and a distinct craniofacial dysmorphism. Similar but less pronounced craniofacial features were present in the mildly mentally retarded mother. This observation confirms a previous report of a boy with the same MCA-MR syndrome and suggests X linked or autosomal dominant inheritance.
我们报告了一名患有严重智力发育迟缓、中枢神经系统畸形、外胚层发育不良体征以及明显颅面畸形的儿童。轻度智力发育迟缓的母亲也有类似但不太明显的颅面特征。这一观察结果证实了之前关于一名患有相同MCA-MR综合征男孩的报告,并提示其遗传方式为X连锁或常染色体显性遗传。