Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models

Abstract excerpt

Laminin a2 gene (LAMA2)-related Congenital Muscular Dystrophy was distinguished by a defining central nervous system (CNS) abnormality - aberrant white matter signals by MRI - when first described in the 1990s. In the past 25 years, researchers and clinicians have expanded our knowledge of brain involvement in LAMA2-related Congenital Muscular Dystrophy (CMD), also known as Congenital Muscular Dystrophy Type 1A...

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