Late-onset distal muscular dystrophy affecting the posterior calves

Jonathan S. Katz, Thomas A. Rando, Richard J. Barohn, David S. Saperstein, Carlayne E. Jackson, Matthew Wicklund, Anthony A. Amato

Producción científica: Articlerevisión exhaustiva

16 Citas (Scopus)

Resumen

Miyoshi myopathy, caused by mutations in the membrane protein dysferlin, is the most common muscular dystrophy that presents in the posterior calves. Its onset is before the age of 30 years and it is associated with marked elevations of serum creatine kinase (CK). In contrast, little is known about calf myopathies with onset after the age of 30, and it is not clear whether such patients have a dysferlinopathy. We describe five patients with a myopathy predominantly affecting the calf muscles, with onset after the age of 30. Muscle tissue was analyzed by immunoblot for dystrophin and dysferlin. All five had normal dysferlin but one had a dystrophinopathy. Serum CK levels ranged from 3 to 15 times the upper limit of normal. In contrast, all of 13 patients presenting before age 30 with calf weakness had a dysferlinopathy. Thus, isolated calf atrophy and weakness with onset after age 30, and associated with serum CK levels that are only moderately elevated, represents a distinct myopathy phenotype. Most of these cases are sporadic, although the overall phenotype appears genetically heterogeneous and dysferlinopathy is uncommon.

Idioma originalEnglish (US)
Páginas (desde-hasta)443-448
Número de páginas6
PublicaciónMuscle and Nerve
Volumen28
N.º4
DOI
EstadoPublished - oct 1 2003

ASJC Scopus subject areas

  • Clinical Neurology
  • Physiology (medical)
  • Cellular and Molecular Neuroscience
  • Physiology

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