An Unusual Case of Nemaline Myopathy Type 3
K. Tripathi, S. Khosa & S. K. Mishra · Journal of Advances in Medicine and Medical Research · 2022
Objective: To report an interesting case of Nemaline Myopathy type 3 with alpha-actin1 (ACTA1) mutation. Background: Nemaline myopathy (NM) is a rare congenital neuromuscular disorder that presents with facial weakness, bulbar symptoms, generalized muscle weakness, delayed motor...
Open access
Research Article
10.9734/jammr/2022/v34i2131538