Congenital muscular dystrophy with severe retrocollis and mental retardation: a report of two siblings

J Neurol Neurosurg Psychiatry. 1997 Mar;62(3):279-81. doi: 10.1136/jnnp.62.3.279.

Abstract

Two siblings with a congenital muscular dystrophy and severe mental retardation which was not due to dystrophin, merosin, or adhalin deficiency are described. These cases overlap with congenital muscular dystrophy of the Fukuyama-type but are less severe. Atypical features include limited facial involvement, retained ambulation, and severe retrocollis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Humans
  • Intellectual Disability*
  • Male
  • Muscular Dystrophies / congenital*
  • Nuclear Family
  • Torticollis*