Pediatric Neurology Briefs (May 2013)

Coats Syndrome in Facioscapulohumeral Dystrophy Type 1

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-27-5-2
Journal volume & issue
Vol. 27, no. 5
pp. 34 – 35

Abstract

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Investigators at University of Rochester Medical Center, NY; Hopital Archet-CHU de Nice, France; and Albert Einstein College of Medicine, NY, studied the frequency of Coats syndrome and its association with D4Z4 contraction size in 408 patients identified with facioscapulohumeral dystrophy type 1 (FSHD1).

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