| Literature DB >> 18054699 |
Berten P Ceulemans1, Katrien Storm, Edwin Reyniers, Luc Callewaert, Jean Jacques Martin.
Abstract
We present a family with dystrophinopathy in whom the proband is a female aged 4.5 years, who presented with exertional muscle pain without weakness. Familial analysis identified a maternal nephew of the proband who demonstrated a similar clinical picture, with asymptomatic cardiomyopathy. A DNA analysis revealed an in-frame deletion in the proximal part of domain II of the dystrophin gene. Extensive familial analysis indicated that the asymptomatic maternal grandfather transmitted the deletion. This is the first report of a young female patient with exertional muscle pain as the only early presenting symptom of dystrophinopathy.Entities:
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Year: 2008 PMID: 18054699 DOI: 10.1016/j.pediatrneurol.2007.09.006
Source DB: PubMed Journal: Pediatr Neurol ISSN: 0887-8994 Impact factor: 3.372