Oropharyngeal dysphagia may occur in late-onset Pompe disease, implicating bulbar muscle involvement.
Abstract
Late-onset Pompe disease (presenting after 12 months of age) often presents with limb-girdle
and respiratory weakness, but oropharyngeal dysphagia has not been reported previously.
A retrospective review of all late-onset Pompe disease patients evaluated in the neuromuscular
clinic at Duke University Medical Center from 1999-2010 was performed. Twelve patients
were identified and 3 had symptoms of oropharyngeal dysphagia. The medical record
was reviewed, including the results of electromyography, videofluroscopic swallow
examinations, and motor speech examination including instrumental assessment of lingual
force with the Iowa Oral Performance Instrument. Oropharyngeal dysphagia was mild
in two cases and severe in one. One of the two patients with mild severity demonstrated
oral stage swallow signs; in the other, residual material was observed in the area
of the cervical esophagus. In the patient with severe oropharyngeal dysphagia, both
the oral and pharyngeal stages of swallowing were affected with penetration and aspiration
documented. The degree of swallowing impairment appeared to correlate with overall
physical strength and function. Oropharyngeal dysphagia may occur in patients with
late-onset Pompe disease, implicating bulbar muscle involvement. Screening for symptoms
of dysphagia may help reduce morbidity and mortality, while improving understanding
of the late-onset Pompe disease phenotype. Further studies, including examination
of the relationship between lingual weakness and oropharyngeal dysphagia, are warranted.
Type
Journal articleSubject
HumansDeglutition Disorders
Glycogen Storage Disease Type II
Electromyography
Retrospective Studies
Adult
Middle Aged
Female
Male
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https://hdl.handle.net/10161/27311Published Version (Please cite this version)
10.1016/j.nmd.2012.12.003Publication Info
Hobson-Webb, Lisa D; Jones, Harrison N; & Kishnani, Priya S (2013). Oropharyngeal dysphagia may occur in late-onset Pompe disease, implicating bulbar
muscle involvement. Neuromuscular disorders : NMD, 23(4). pp. 319-323. 10.1016/j.nmd.2012.12.003. Retrieved from https://hdl.handle.net/10161/27311.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Lisa Deneen Hobson-Webb
Professor of Neurology
Trained in neuromuscular medicine, my clinical career has focused on the care of patients
with genetically mediated neuromuscular disorders, rare peripheral neuropathies, and
immune-mediated nerve and muscle disorders and performing high quality electrodiagnostic
testing (nerve conduction studies/electromyography). As a researcher, the core aim
of my work is applying high resolution ultrasound in the care of patients with neuromuscular
diseases. My early work focused on peripheral nerve
Harrison N. Jones
Associate Professor of Head and Neck Surgery & Communication Sciences
Priya Sunil Kishnani
Chen Family Distinguished Professor of Pediatrics
RESEARCH INTERESTS A multidisciplinary approach to care of individuals with genetic
disorders in conjunction with clinical and bench research that contributes to: 1)
An understanding of the natural history and delineation of long term complications
of genetic disorders with a special focus on liver Glycogen storage disorders, lysosomal
disorders with a special focus on Pompe disease, Down syndrome and hypophosphatasia2) )
The development of new therapies such
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