The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more

Citation
Es. Gordon et Ep. Hoffman, The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more, CURR OP NEU, 14(5), 2001, pp. 567-573
Citations number
39
Categorie Soggetti
Neurology
Journal title
CURRENT OPINION IN NEUROLOGY
ISSN journal
13507540 → ACNP
Volume
14
Issue
5
Year of publication
2001
Pages
567 - 573
Database
ISI
SICI code
1350-7540(200110)14:5<567:TAOLMD>2.0.ZU;2-G
Abstract
Limb-girdle muscular dystrophy is a class of disorders encompassing many fo rms of this disease. Variation exists between the inheritance patterns, gen es responsible, course of disease and symptoms, with the cohesive factor am ong these disorders being the predominance of proximal muscle weakness. Her e we review each form of limb-girdle muscular dystrophy with attention to m olecular genetics, clinical features, inheritance, and diagnostic issues pe rtaining to each primary genetic cause. Curr Opir Neurol 14:567-573. (C) 20 01 Lippincott Williams & Wilkins.