Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation.

Autor: Al-Futaisi AM; Department of Child Health, Sultan Qaboos University Hospital, Sultan Qaboos University, Muscat, Oman., Al-Kindi MN, Al-Mawali AM, Koul RL, Al-Adawi S, Al-Yahyaee SA
Jazyk: angličtina
Zdroj: Pediatric neurology [Pediatr Neurol] 2012 Feb; Vol. 46 (2), pp. 89-93.
DOI: 10.1016/j.pediatrneurol.2011.11.008
Abstrakt: Hyperekplexia is characterized by neonatal hypertonia and exaggerated startle reflex in response to loud noise or tactile stimuli. Mutations in patients with hyperekplexia were evident in several genes encoding proteins involved in glycinergic neurotransmission, i.e., glycine receptor α and β subunits, collybistin, gephyrin, and glycine transporter 2. We clinically and genetically characterized two large, unrelated consanguineous families with hyperekplexia. Affected members of the two families manifested hyperekplexia with mild mental retardation. Patients exhibited a novel homozygote c.593G>C missense mutation in GLRA1, resulting in amino acid substitution p.W170S in the corresponding mature glycine receptor α1 subunit. This mutation was absent in 400 randomly selected chromosomes in the same population. In conclusion, a novel p.W170S mutation in the extracellular ligand binding domain of glycine receptor α1 subunit was detected in patients with hyperekplexia and mild mental retardation.
(Published by Elsevier Inc.)
Databáze: MEDLINE
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