Limb-Girdle Muscular Dystrophy Type 2C Overview
Learn About Limb-Girdle Muscular Dystrophy Type 2C
- Limb-girdle muscular dystrophy, type 2C
- Adhalin deficiency, secondary
- Autosomal recessive limb-girdle muscular dystrophy type 2C
- DMDA
- DMDA1
- Duchenne-like muscular dystrophy, autosomal recessive, type 1
- Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5
- Gamma-sarcoglycan-related LGMD R5
- Gamma-sarcoglycanopathy
- LGMD due to gamma-sarcoglycan deficiency
- LGMD type 2C
- LGMD2C
- Limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency
- Limb-girdle muscular dystrophy type 2C
- Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency
- Maghrebian myopathy
- Muscular dystrophy, Duchenne-like
- Severe childhood autosomal recessive muscular dystrophy, North African type
State University Of Iowa
Katherine Mathews is a Neurologist and a Pediatrics provider in Iowa City, Iowa. Dr. Mathews is rated as a Distinguished provider by MediFind in the treatment of Limb-Girdle Muscular Dystrophy Type 2C. Her top areas of expertise are Limb-Girdle Muscular Dystrophy Type 2I, Limb-Girdle Muscular Dystrophy, Dystrophinopathy, and Friedreich Ataxia. Dr. Mathews is currently accepting new patients.
Aurora Family Medicine
Brian Demaster is a primary care provider, practicing in Family Medicine in Cedar Grove, Wisconsin. Dr. Demaster is rated as an Experienced provider by MediFind in the treatment of Limb-Girdle Muscular Dystrophy Type 2C. His top areas of expertise are Limb-Girdle Muscular Dystrophy Type 1A, Limb-Girdle Muscular Dystrophy Type 2C, Limb-Girdle Muscular Dystrophy Type 2I, and Limb-Girdle Muscular Dystrophy Type 2B.
Advocate Medical Group Neurology
David Randall is a Neurologist in Park Ridge, Illinois. Dr. Randall is rated as an Advanced provider by MediFind in the treatment of Limb-Girdle Muscular Dystrophy Type 2C. His top areas of expertise are Lambert-Eaton Syndrome, Peripheral Neuropathy, Chronic Inflammatory Demyelinating Polyneuropathy, and Myasthenia Gravis.
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center

