Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters











Database
Language
Publication year range
1.
Rev Med Chil ; 128(7): 772-7, 2000 Jul.
Article in Spanish | MEDLINE | ID: mdl-11050839

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.


Subject(s)
Dystrophin/genetics , Exercise , Muscular Dystrophies/complications , Pain/etiology , Blotting, Western , Child , Creatine Kinase/blood , Exons/genetics , Gene Deletion , Humans , Male , Muscular Dystrophies/genetics , Polymerase Chain Reaction
SELECTION OF CITATIONS
SEARCH DETAIL