Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome

J Med Genet. 1996 Mar;33(3):224-6. doi: 10.1136/jmg.33.3.224.

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.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Brain / abnormalities*
  • Brain / diagnostic imaging
  • Child, Preschool
  • Ectoderm / pathology
  • Facial Bones / abnormalities*
  • Female
  • Genes, Dominant
  • Humans
  • Infant, Newborn
  • Infant, Premature
  • Intellectual Disability / genetics*
  • Male
  • Pregnancy
  • Skull / abnormalities*
  • Syndrome
  • Tomography, X-Ray Computed
  • X Chromosome