Literature DB >> 21183346

A case of adult Pompe disease presenting with severe fatigue and selective involvement of type 1 muscle fibers.

Linda E M van den Berg1, Juna M de Vries, Robert M Verdijk, Ans T van der Ploeg, Arnold J J Reuser, Pieter A van Doorn.   

Abstract

We present a case of adult Pompe disease (acid maltase deficiency) with an uncommon clinical presentation characterized by severe fatigue and myalgia prior to the onset of limb girdle weakness. Remarkably, the muscle biopsy demonstrated selective involvement of type 1 muscle fibers. The cause and clinical effects of fiber type specific involvement are currently unknown, but the phenomenon might contribute to the clinical heterogeneity in Pompe disease and the variable response to enzyme replacement therapy.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21183346     DOI: 10.1016/j.nmd.2010.11.016

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  2 in total

1.  Muscle fiber-type distribution, fiber-type-specific damage, and the Pompe disease phenotype.

Authors:  L E M van den Berg; M R Drost; G Schaart; J de Laat; P A van Doorn; A T van der Ploeg; A J J Reuser
Journal:  J Inherit Metab Dis       Date:  2012-10-11       Impact factor: 4.982

2.  Lack of robust satellite cell activation and muscle regeneration during the progression of Pompe disease.

Authors:  Gerben J Schaaf; Tom J M van Gestel; Esther Brusse; Robert M Verdijk; Irenaeus F M de Coo; Pieter A van Doorn; Ans T van der Ploeg; W W M Pim Pijnappel
Journal:  Acta Neuropathol Commun       Date:  2015-10-28       Impact factor: 7.801

  2 in total

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