## Abstract Epilepsy and electroencephalogram (EEG) abnormalities have been considered exclusion criteria for the clinical diagnosis of myoclonusโdystonia (MโD). We report on the second MโD family in which several clinically affected ฯตโsarcoglycan gene (SGCE) mutation carriers have seizures in addi
โฆ LIBER โฆ
Hereditary myoclonus-dystonia associated with epilepsy
โ Scribed by Foncke, E. M.J.; Klein, C.; Koelman, J. H.T.M.; Kramer, P. L.; Schilling, K.; Muller, B.; Garrels, J.; de Carvalho Aguiar, P.; Liu, L.; de Froe, A.; Speelman, J. D.; Ozelius, L. J.; Tijssen, M. A.J.
- Book ID
- 118167186
- Publisher
- Lippincott Williams and Wilkins
- Year
- 2003
- Tongue
- English
- Weight
- 204 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0028-3878
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## Abstract Because of clinical similarities, benign hereditary chorea and myoclonusโdystonia (DYT11) might be confused. No systematic comparisons of genetically proven cases with thyroid transcription factorโ1 (__TITFโ1__) and ฮตโsarcoglycan (__SGCE__) mutations have been performed to date. Three i
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