A Case of a Newborn With Nemaline Myopathy From Al-Qunfudhah City, Saudi Arabia.

Nemaline myopathy is a primary skeletal muscle disorder and one of the congenital myopathies. It can be caused by mutations in at least 12 genes, with the () gene being the most common. Here, we present the first case of a neonate with nemaline myopathy from Al-Qunfudhah, Saudi Arabia.