1. Paroxysmal exercise-induced dyskinesia with self-limiting partial epilepsy: A novel GLUT-1 mutation with benign phenotype
- Author
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Alfonso Fasano, Elena Fontana, Ina Juergenson, Michele Tinazzi, Barbara Castellotti, Cinzia Gellera, and Tommaso Bovi
- Subjects
Adult ,medicine.medical_specialty ,Paroxysmal exercise-induced dystonia ,paroxysmal exercise-induced dystonia ,epilepsy ,GLUT-1 deficiency syndrome ,Epilepsy, Partial, Motor ,Bioinformatics ,medicine.disease_cause ,Polymerase Chain Reaction ,Epilepsy ,Chorea ,Internal medicine ,medicine ,Humans ,Point Mutation ,Exercise ,Dystonia ,Mutation ,business.industry ,Glucose transporter ,Carbamazepine ,Paroxysmal dyskinesia ,medicine.disease ,Phenotype ,Endocrinology ,Excitatory Amino Acid Transporter 2 ,Neurology ,Dyskinesia ,Female ,Neurology (clinical) ,Geriatrics and Gerontology ,medicine.symptom ,business ,medicine.drug - Abstract
Paroxysmal exercise-induced dyskinesia (PED) is a rare form of dystonia induced by prolonged exercise, usually involving lower limbs. PED has been recently described as a possible clinical manifestation of mutations of SLC2A1 gene, encoding for the glucose transport GLUT-1. We report a case of a young woman with a mild form of PED associated with self-limiting partial epilepsy. She carries a novel sporadic heterozygous mutation of the SLC2A1 gene. Diagnostic difficulties and possible treatment with carbamazepine are discussed.
- Published
- 2011
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