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Article

Coats syndrome in facioscapulohumeral dystrophy type 1: frequency and D4Z4 contraction size.

Neurology - 26 Mar 2013

Statland Jeffrey M, Sacconi Sabrina, Farmakidis Constantine, Donlin-Smith Colleen M, Chung Mina, Tawil Rabi

Abstract excerpt

OBJECTIVE: To investigate the frequency of Coats syndrome and its association with D4Z4 contraction size in patients with facioscapulohumeral muscular dystrophy type 1 (FSHD1). METHODS: We searched a North American FSHD registry and the University of Rochester (UR) FSHD research database, reviewed the literature, and sent surveys to 14 FSHD referral centers in the United States and overseas to identify patients...

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Share to Chromosomes, Human, Pair 4
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Muscular Dystrophy, Facioscapulohumeral

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Source

Open in PubMed Open full text

Identifiers

PMID: 23446679
DOI: 10.1212/WNL.0b013e3182897116
PMCID: PMC3691782

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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