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

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Date

2011-12

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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.

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Subjects

Humans, Muscle Weakness, Tongue Diseases, Glycogen Storage Disease Type II, Age of Onset, Phenotype, Adolescent, Adult, Aged, Middle Aged, Female, Male, Young Adult

Citation

Published Version (Please cite this version)

10.1002/mus.22202

Publication Info

Dubrovsky, Alberto, Jose Corderi, Min Lin, Priya S Kishnani and Harrison N Jones (2011). Expanding the phenotype of late-onset Pompe disease: tongue weakness: a new clinical observation. Muscle & nerve, 44(6). pp. 897–901. 10.1002/mus.22202 Retrieved from https://hdl.handle.net/10161/27317.

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