| Literature DB >> 8728696 |
K Devriendt1, L D'Espallier, J P Fryns.
Abstract
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.Entities:
Mesh:
Year: 1996 PMID: 8728696 PMCID: PMC1051872 DOI: 10.1136/jmg.33.3.224
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318