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Paroxysmal Exercise-induced Dyskinesias Caused by GLUT1 Deficiency Syndrome
Marie Mongin1, Nicolas Mezouar2, Pauline Dodet3
1CHRU de Tours, Hôpital Bretonneau, Service de Neurologie, Tours, France; Université François Rabelais de Tours, Tours, France; Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.
Background:
Glucose transporter type 1 deficiency syndrome is due to de novo mutations in the SLC2A1 gene encoding the glucose transporter type 1.
Phenomenology Shown:
Paroxysmal motor manifestations induced by exercise or fasting may be the main manifestations of glucose transporter type 1 deficiency syndrome.
Educational Value:
Proper identification of the paroxysmal events and early diagnosis is important since the disease is potentially treatable.
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