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Artigo em Russo | MEDLINE | ID: mdl-8154209

RESUMO

Dystrophic myotonia is a sufficiently rare disease inherited mainly by the autosomal dominant type. Clinical picture is characterized by the myotonic, myopathic, and endocrine-autonomic syndrome. A clinical, genetic, and electromyographic study was carried out to elucidate the problem of this condition inheritance, its intra- and interfamilial clinical polymorphism, and effects of environmental factors on its course and outcomes.


Assuntos
Distrofia Miotônica/diagnóstico , Adulto , Eletromiografia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Distrofia Miotônica/genética , Linhagem , Polimorfismo Genético
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