Child Neurology: LAMA2 muscular dystrophy without contractures

We present an interesting case with a novel mutation in the laminin α2 (LAMA2) gene, which has not been reported previously; the patient has a mixed clinical phenotype without contractures.

Source: Neurology - May 22, 2017 Category: Neurology Authors: Dean, M., Rashid, S., Kupsky, W., Moore, S. A., Jiang, H. Tags: All Neuromuscular Disease, Muscle disease, All Pediatric RESIDENT AND FELLOW SECTION Source Type: research