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Updated: Sep 3, 2025

Behavioral and Locomotor Measurements Using an Open Field Activity Monitoring System for Skeletal Muscle Diseases
Published on: September 29, 2014
LAMA2-related muscular dystrophy mimicking multiple sclerosis
Jacqueline Koshorek1, Nara de Macena Sobreira2, Shiv Saidha3
1Neuroimmunology and Neurological Infections, Johns Hopkins University, Baltimore, Maryland, USA koshorekjacqueline@gmail.com.
Late-onset LAMA2-related muscular dystrophy (LAMA2-MD) can mimic multiple sclerosis, presenting with spinal cord abnormalities. Genetic testing is crucial for diagnosing this rare condition and ensuring appropriate patient management.
Area of Science:
- Neurology
- Genetics
- Muscular Dystrophy
Background:
- Laminin-alpha2-related muscular dystrophy (LAMA2-MD) is a genetic disorder impacting the nervous system.
- Late-onset LAMA2-MD presents with varied symptoms including muscle weakness, neuropathy, and neurological issues, distinct from the neonatal form.
- This study highlights a rare LAMA2-MD phenotype involving progressive myelopathy and spinal cord abnormalities.
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