Emery-Dreifuss syndrome: genetic and clinical varieties

Am J Med Genet. 1994 Apr 15;50(3):228-33. doi: 10.1002/ajmg.1320500304.

Abstract

Two familial and 2 sporadic cases of Emery-Dreifuss syndrome are reported. One family presented a rare autosomal dominant variant of Emery-Dreifuss muscular dystrophy, another with X-linked recessive inheritance showed unusual intrafamilial variability. One of sporadic cases closely resembled rigid spine syndrome, the other was clinically intermediate between Emery-Dreifuss muscular dystrophy and rigid spine syndrome, showing that they are not distinct disorders.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Contracture / genetics
  • Female
  • Genes, Dominant
  • Heart Block / genetics
  • Humans
  • Infant, Newborn
  • Male
  • Muscular Atrophy / genetics
  • Muscular Dystrophies / classification
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / pathology
  • Pedigree
  • Phenotype
  • Syndrome
  • X Chromosome