Clinical and histopathological heterogeneity in patients with 4q35 facioscapulohumeral muscular dystrophy (FSHD)

Neuropathol Appl Neurobiol. 2004 Apr;30(2):188-91. doi: 10.1046/j.0305-1846.2003.00520.x.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Chromosomes, Human, Pair 4 / genetics
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Microscopy, Electron
  • Middle Aged
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology*
  • Muscle, Skeletal / ultrastructure
  • Muscular Dystrophy, Facioscapulohumeral / genetics*
  • Muscular Dystrophy, Facioscapulohumeral / physiopathology*
  • Pedigree
  • Phenotype