Coats Syndrome in Facioscapulohumeral Dystrophy Type 1

J Gordon Millichap

doi:10.15844/pedneurbriefs-27-5-2

Coats Syndrome in Facioscapulohumeral Dystrophy Type 1

Pediatric Neurology Briefs

Volume 27 (2013): Issue 5

By: J Gordon Millichap

Open Access

|May 2013

Abstract

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).

References

Statland JM Sacconi S Farmakidis C Donlin-Smith CM Chung M Tawil R Coats syndrome in facioscapulohumeral dystrophy type 1 Neurology 2013 Mar 26 80 13 1247 50 10.1212/WNL.0b013e3182897116 23446679
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Coats G Forms of retinal disease with massive exudation Royal London Ophthalmic Hospital Reports 1908 17 3 440 525
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Small RG Coats’ disease and muscular dystrophy Transactions of the American Academy of Ophthalmology and Oto-Laryngology, Rochester, MN 1968 72 2 225 31 5659903
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-27-5-2 | Journal eISSN: 2166-6482

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Language: English

Page range: 34 - 35

Published on: May 1, 2013

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Facioscapulohumeral Dystrophy,

Coats Disease,

Exudative Retinitis

© 2013 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 27 (2013): Issue 5