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Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency.
Vattemi, Gaetano; Neri, Marcella; Marini, Matteo; Gualandi, Francesca; Tonin, Paola; Bertolasi, Laura; Guglielmi, Valeria; Catalli, Claudio; Novelli, Giuseppe; Ferlini, Alessandra; Tomelleri, Giuliano.
Afiliação
  • Vattemi G; Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy.
Neurologist ; 18(5): 306-9, 2012 Sep.
Article em En | MEDLINE | ID: mdl-22931740
ABSTRACT

INTRODUCTION:

Calpain 3 deficiency causes limb girdle muscular dystrophy type 2A, which is one of the most common forms of limb girdle muscular dystrophy. Nevertheless, calpainopathy is not always associated with mutations in the specific gene and secondary reduction in protein expression has been described. CASE REPORT We report a case of a 43-year-old man who complained of thigh muscle stiffness and had muscle hypertrophy of both vastus medialis with prolonged myotonic contraction by percussion. A muscle biopsy showed dystrophic features and calpain 3 deficiency was shown by immunoblot analysis although mutations in the specific gene were not found. Known cases of secondary calpain 3 protein deficiency were ruled out and mutations in MD1 and MD2 genes were excluded.

CONCLUSIONS:

This patient represents the first case of calpain 3 deficiency with selective pseudohypertrophy of vastus medialis muscles.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Calpaína / Distrofia Muscular do Cíngulo dos Membros / Músculo Quadríceps / Proteínas Musculares Tipo de estudo: Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Calpaína / Distrofia Muscular do Cíngulo dos Membros / Músculo Quadríceps / Proteínas Musculares Tipo de estudo: Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2012 Tipo de documento: Article