Dysphagia-related quality of life in oculopharyngeal muscular dystrophy: Psychometric properties of the SWAL-QOL instrument

Author:

Youssof Sarah1,Romero-Clark Carol2,Warner Teddy3,Plowman Emily4

Affiliation:

1. Department of Neurology, MSC 10 5620, 1; University of New Mexico Health Sciences Center; Albuquerque New Mexico 87131 USA

2. Speech, Language, Swallow Center; University of New Mexico Health Sciences Center; Albuquerque New Mexico USA

3. Department of Family and Community Medicine; University of New Mexico Health Sciences Center; Albuquerque New Mexico USA

4. Speech, Language and Hearing Sciences, Center for Respiratory Research & Rehabilitation; University of Florida; Gainesville Florida USA

Funder

Muscular Dystrophy Association

NCATS

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference40 articles.

1. Oculopharyngeal muscular dystrophy. A familial disease of late life characterized by dysphagia and progressive ptosis of the evelids;Victor;N Engl J Med,1962

2. Oropharyngeal dysphagia in patients with oculopharyngeal muscular dystrophy;Duranceau;Can J Surg,1978

3. Oculopharyngeal muscular dystrophy;Brais;Handb Clin Neurol,2011

4. Interventions for dysphagia in long-term, progressive muscle disease;Jones;Cochrane Database Syst Rev,2016

5. Manometric and radionuclide assessment of pharyngeal emptying before and after cricopharyngeal myotomy in patients with oculopharyngeal muscular dystrophy;Taillefer;J Thorac Cardiovasc Surg,1988

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