Headache in juvenile myoclonic epilepsy
✍ Scribed by Christoph J. Schankin; Jan Rémi; Ira Klaus; Petra Sostak; Veronika M. Reinisch; Soheyl Noachtar; Andreas Straube
- Publisher
- Springer
- Year
- 2011
- Tongue
- English
- Weight
- 184 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1129-2369
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We examined the inheritance of juvenile myoclonic epilepsy (JME). We looked at both the trait of "epilepsy" and the trait of "epilepsy-plus-EEG abnormalities," since EEG abnormalities are frequently found in the clinically unaffected sibs of JME patients. We tested several modes of inheritance inclu
We undertook genetic study of patients with juvenile myoclonic epilepsy (JME) from 17 families. There was a mean of 8 children in each sibship. Siblings were affected in 8 sibships, and some families had more than 2 members affected by JME. Half-siblings and parental involvement were found in only 1