Literature DB >> 11050839

[Post exercise myalgias as presentation form of dystrophinopathy].

K Kleinsteuber1, P Rocco, L Herrera, M Vainzof, M E Birke, M Yáñez, A Flandes, M Zatz, P de Carvallo, M A Avaria.   

Abstract

Cramps and myalgias are frequent presentations of many disorders whose diagnosis is generally difficult. Among the unusual causes stand the milder phenotypes of dystrophinopathies, which are caused, just as Duchenne and Becker's dystrophy, by mutations in the dystrophin gene. An 8 year-old boy presented severe muscle pain on exercise and serum rise in creatine kinase over 1000 U/l. He had normal muscle power and mild calf hypertrophy. The molecular analysis by polymerase chain reaction (PCR) of the dystrophin gene showed deletions of exons 45 to 51. Dystrophin analysis by Western blot revealed a dystrophin of reduced quantity and molecular weight. Emphasis is made to include dystrophinopathies in the differential diagnosis of myalgias and the usefulness of molecular genetic techniques in the identification of these disorders.

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Year:  2000        PMID: 11050839

Source DB:  PubMed          Journal:  Rev Med Chil        ISSN: 0034-9887            Impact factor:   0.553


  2 in total

1.  Pseudometabolic presentation of dystrophinopathy due to a missense mutation.

Authors:  Aravindhan Veerapandiyan; Vandana Shashi; Yong-Hui Jiang; William Brian Gallentine; Kelly Schoch; Edward Clinton Smith
Journal:  Muscle Nerve       Date:  2010-12       Impact factor: 3.217

2.  Commentary to medical genetics and genomic medicine in Chile: Chilean experience on molecular diagnosis for neurodegenerative disorders.

Authors:  Marcelo Miranda; María Leonor Bustamante
Journal:  Mol Genet Genomic Med       Date:  2017-05-02       Impact factor: 2.183

  2 in total

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