We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Dystonic tremor caused by mutation of the glucose transporter gene GLUT1.
- Authors
Roubergue, Anne; Apartis, Emmanuelle; Mesnage, Valérie; Doummar, Diane; Trocello, Jean-Marc; Roze, Emmanuel; Taieb, Guillaume; De Villemeur, Thierry Billette; Vuillaumier-Barrot, Sandrine; Vidailhet, Marie; Levy, Richard
- Abstract
Glucose transporter 1 deficiency syndrome (GLUT1-DS) is due to heterozygous mutation of the glucose transporter type 1 gene (GLUT1/SLC2A1). GLUT1-DS is characterized by movement disorders, including paroxysmal exercise-induced dystonia (PED), as well as seizures, mental retardation and hypoglycorrhachia. Tremor was recently shown to be part of the phenotype, but its clinical and electrophysiological features have not yet been described in detail, and GLUT1 tremor reports are rare. We describe two patients, a young woman and her mother, who were referred to us for tremor. We also systematically review published cases of GLUT1-DS with tremor (14 cases, including ours), focusing on clinical features. In most cases (10/14), the tremor, which involved the limbs and voice, fulfilled clinical criteria for dystonic tremor (DT), occurring in body areas affected by dystonia. Tremor was the only permanent symptom in 2 cases. Recordings, reported here for the first time, showed an irregular 6- to 8.5-Hz tremor compatible with DT in our two patients. These findings show that tremor, and particularly DT, may be a presenting symptom of GLUT1-DS. Patients who present with dystonic tremor, with or without mental retardation, seizures, movement disorders and/or a family history, should therefore be screened for GLUT1-DS.
- Publication
Journal of inherited metabolic disease, 2011, Vol 34, Issue 2, p483
- ISSN
1573-2665
- Publication type
Journal Article
- DOI
10.1007/s10545-010-9264-6