Limb-girdle muscular dystrophy, type 2C
- Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency
- Muscular dystrophy, Duchenne-like
- Duchenne-like muscular dystrophy, autosomal recessive, type 1
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There is no specific treatment for limb-girdle muscular dystrophy. Management of the condition is based on the person's symptoms and subtype (if known). The GeneReview article on limb-girdle muscular dystrophy lists the following approach for medical management of the condition:
- Weight control to avoid obesity
- Physical therapy and stretching exercises to promote mobility and prevent contractures
- Use of mechanical aids such as canes, walkers, orthotics, and wheelchairs as needed to help ambulation and mobility
- Monitoring and surgical intervention as needed for orthopedic complications such as foot deformity and scoliosis
- Monitoring of respiratory function and use of respiratory aids when indicated
- Monitoring for evidence of cardiomyopathy in those subtypes with known occurrence of cardiac involvement
- Social and emotional support and stimulation to maximize a sense of social involvement and productivity and to reduce the sense of social isolation common in these disorders
- Gordon E, Pegoraro E, Hoffman EP. Limb-Girdle Muscular Dystrophy Overview. Gene Reviews. September 2, 2008; http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lgmd-overview. Accessed 4/14/2009.
- Finding Treatment Information - A video developed by GARD Information Specialists that explains how you can find information about treatment for a rare disease.
- GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.
- ClinicalTrials.gov lists trials that are studying or have studied Limb-girdle muscular dystrophy, type 2C. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
- Orphanet lists European clinical trials, research studies, and patient registries enrolling people with this condition.