Sleep Disorder: An Overlooked Manifestation of Glucose Transporter Type-1 Deficiency Syndrome.

Glucose transporter type-1 deficiency syndrome, familial Glut1 DS, sleep disorder, seizure, daytime somnolence, paroxysmal exercise-induced dyskinesia Keywords: glucose transporter type-1 deficiency syndrome; familial Glut1 DS; sleep disorder; daytime somnolence; seizure; paroxysmal exercise-induced dyskinesia EN glucose transporter type-1 deficiency syndrome familial Glut1 DS sleep disorder daytime somnolence seizure paroxysmal exercise-induced dyskinesia 129 132 4 04/21/22 20220301 NES 220301 Conflict of Interest The authors declare no competing interests. Glut1 deficiency syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group. Introduction Glucose transporter type-1 deficiency syndrome (Glut1 DS) is a rare genetic-metabolic disorder caused by mutations in the I SLC2A1 i gene on chromosome 1p34.2. [Extracted from the article]

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