Limb-Girdle Muscular Dystrophy EXPLORE Module


Activity Info

There are 35 genetic subtypes of Limb-Girdle Muscular Dystrophy (LGMD). An early diagnosis is critical for appropriate patient surveillance and monitoring. Gene therapy is being explored for the most common LGMD subtypes. Learn about clinical trials for emerging therapies, genetic testing for diagnosis, and recommended referral pathways for patients with LGMD from experts Dr. Carla Zingariello and Dr. Peter Kang.

CME/CE Information is available in the activity.


Webinar | Video | CME (AMA PRA Category 1 Credit) | 1.0 - 60 mins | Interactive Case | Genetic Counselor | Neurology | Neuromuscular Specialist | Pediatrics | Family Medicine | Nurse | Nurse Practitioner | Physical Medicine & Rehabilitation | Limb Girdle Muscle Weakness (LGMW) | Genomic Medicine | Orthopedic Surgery | Physician Assistant | Muscular Dystrophy | Duchenne Muscular Dystrophy (DMD) | AAPA | ANCC | 

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