Ontology highlight
ABSTRACT:
SUBMITTER: Khaiboullina SF
PROVIDER: S-EPMC5406743 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature
Khaiboullina Svetlana F SF Martynova Ekaterina V EV Bardakov Sergey N SN Mavlikeev Mikhail O MO Yakovlev Ivan A IA Isaev Arthur A AA Deev Roman V RV Rizvanov Albert A AA
Case reports in medicine 20170413
Limb-girdle muscular dystrophy type 2 (LGMD2B) is a mild form of dysferlinopathy, characterized by limb weakness and wasting. It is an autosomal recessive disease, with currently 140 mutations in the LGMD2B gene identified. Lack of functional dysferlin inhibits muscle fiber regeneration in voluntary muscles, the main pathological finding in LGMD2B patients. However, the immune system has been suggested to contribute to muscle cell death and tissue regeneration. Serum levels of 27 cytokines were ...[more]