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LIMBGIRDLE MUSCULAR DYSTROPHY DUE TO SARCOGLYCAN DEFICIENCY REGISTRYThe questions in the questionnaire pertain to each individual affected by Limbgirdle Muscular Dystrophy due to Sarcoglycan deficiency
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Muscular dystrophy is due to genetic mutations that affect the muscles' ability to function properly.
Individuals with muscular dystrophy or their guardians may be required to file relevant medical documentation or claims for insurance purposes.
To fill out documentation related to muscular dystrophy, gather all medical records, diagnosis details, and follow the specific instructions provided by the relevant institution or insurance provider.
The purpose of documenting muscular dystrophy is to ensure appropriate medical care, management of the condition, and potential access to support services.
The reported information must include patient identification, diagnosis, symptoms, medical history, and current treatment plans.
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