Expanding the phenotype of late-onset Pompe disease: tongue weakness: a new clinical observation.

dc.contributor.author

Dubrovsky, Alberto

dc.contributor.author

Corderi, Jose

dc.contributor.author

Lin, Min

dc.contributor.author

Kishnani, Priya S

dc.contributor.author

Jones, Harrison N

dc.date.accessioned

2023-05-02T13:40:21Z

dc.date.available

2023-05-02T13:40:21Z

dc.date.issued

2011-12

dc.date.updated

2023-05-02T13:40:21Z

dc.description.abstract

Introduction

Following the clinical observation of lingual weakness in 2 patients with late-onset Pompe disease (LOPD), tongue strength was assessed in 19 consecutive patients to determine the frequency and severity of this neurological sign.

Methods

Lingual strength was assessed using manual muscle testing; if weakness was present, severity was established as mild, moderate, or severe.

Results

All the patients exhibited lingual weakness, even 2 asymptomatic patients with a positive family history. Weakness was mild in 12 (63%), moderate in 6 (32%), and severe in 1 (5%). Dysarthria and/or dysphagia were observed or reported in 7 of 19 (37%) patients.

Conclusions

Lingual weakness may be present as an axial sign of LOPD, even relatively early in the disease course, and may contribute to the differential diagnosis of this now treatable condition. Dysphagia and/or dysarthria may also occur. This finding further expands the phenotype of LOPD.
dc.identifier.issn

0148-639X

dc.identifier.issn

1097-4598

dc.identifier.uri

https://hdl.handle.net/10161/27317

dc.language

eng

dc.publisher

Wiley

dc.relation.ispartof

Muscle & nerve

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10.1002/mus.22202

dc.subject

Humans

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Muscle Weakness

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Tongue Diseases

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Glycogen Storage Disease Type II

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Age of Onset

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Phenotype

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Adolescent

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Adult

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Aged

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Middle Aged

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Female

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Male

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Young Adult

dc.title

Expanding the phenotype of late-onset Pompe disease: tongue weakness: a new clinical observation.

dc.type

Journal article

duke.contributor.orcid

Kishnani, Priya S|0000-0001-8251-909X

duke.contributor.orcid

Jones, Harrison N|0000-0002-4171-980X

pubs.begin-page

897

pubs.end-page

901

pubs.issue

6

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

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Basic Science Departments

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Clinical Science Departments

pubs.organisational-group

Institutes and Centers

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Molecular Genetics and Microbiology

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Pediatrics

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Pediatrics, Medical Genetics

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Duke Clinical Research Institute

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Institutes and Provost's Academic Units

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Initiatives

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Duke Innovation & Entrepreneurship

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Head and Neck Surgery & Communication Sciences

pubs.publication-status

Published

pubs.volume

44

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