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 nebulin (NEB) gene being the most common. Here, we present the first case of a neonate with nemaline myopathy from Al-Qunfudhah, Saudi Arabia. A...

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Veröffentlicht in:	Cureus 2024, Vol.16 (1), p.e52523-e52523
Hauptverfasser:	Alghanmi, Bushra M, Alghanmi, Manal M, Alhayli, Mohammed R, Taffour, Randa M, Alghubayshi, Safeyah M
Format:	Report
Sprache:	eng
Online-Zugang:	Volltext
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