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

Muscle Nerve. 2011 Dec;44(6):897-901. doi: 10.1002/mus.22202. Epub 2011 Sep 26.

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.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Aged
  • Female
  • Glycogen Storage Disease Type II / diagnosis*
  • Glycogen Storage Disease Type II / epidemiology
  • Glycogen Storage Disease Type II / physiopathology
  • Humans
  • Male
  • Middle Aged
  • Muscle Weakness / diagnosis*
  • Muscle Weakness / epidemiology
  • Muscle Weakness / physiopathology
  • Phenotype*
  • Tongue Diseases / diagnosis*
  • Tongue Diseases / epidemiology
  • Tongue Diseases / physiopathology
  • Young Adult