Tongue atrophy in facioscapulohumeral muscular dystrophy

Neurology. 2001 Aug 28;57(4):733-5. doi: 10.1212/wnl.57.4.733.

Abstract

Involvement of the lingual muscle is considered one of the exclusion criteria of facioscapulohumeral muscular dystrophy (FSHD). In a series of 151 Japanese patients with 4q35-FSHD, seven patients (4.6%) had tongue atrophy with abnormal MRI findings and typical myogenic patterns of electromyography. All seven patients belong to a group of early-onset FSHD with large gene deletions on chromosome 4q35. Our result suggests that the patients with 4q35-FSHD could have myopathic tongue atrophy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Atrophy
  • Child
  • Chromosomes, Human, Pair 4 / genetics
  • Electromyography
  • Female
  • Gene Deletion
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Muscular Dystrophy, Facioscapulohumeral / genetics
  • Muscular Dystrophy, Facioscapulohumeral / pathology*
  • Tongue / pathology*