Facioscapulohumeral dystrophy associated with hearing loss and coats syndrome

Donald A. Taylor, James E. Carroll, Morton E. Smith, Mary O. Johnson, Glen P. Johnston, Michael H. Brooke

Research output: Contribution to journalArticle

56 Scopus citations

Abstract

Two unrelated cases of infantile facioscapulohumeral dystrophy (FSHD) with Coats syndrome of the retina and sensorineural hearing loss are described. Children with otherwise unexplained visual or hearing deficit should be examined for somatic muscle weakness, which may present only as facial weakness. Early recognition of Coats syndrome in children with FSHD may lead to preservation of vision with appropriate therapy.

Original languageEnglish (US)
Pages (from-to)395-398
Number of pages4
JournalAnnals of Neurology
Volume12
Issue number4
DOIs
StatePublished - Oct 1982
Externally publishedYes

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ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Cite this

Taylor, D. A., Carroll, J. E., Smith, M. E., Johnson, M. O., Johnston, G. P., & Brooke, M. H. (1982). Facioscapulohumeral dystrophy associated with hearing loss and coats syndrome. Annals of Neurology, 12(4), 395-398. https://doi.org/10.1002/ana.410120414