Novel GLRB Gene Mutation in a Saudi Baby with Hyperekplexia
Tamer Mohamed Rizk & Adel Ahmed Hassan Mahmoud · International Neuropsychiatric Disease Journal · 2013
Aim: We aim to describe a case of hyperekplexia in a Saudi neonate due to Novel mutation in GLRB. Case Presentation: One month old Saudi neonate with hypertonicity, repetitive episodes of jitteriness and exaggerated startle reflex. Discussion: Hyperekplexia (OMIM:149400, 138492 &...
Open access
Research Article
10.9734/INDJ/2014/5368