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[Clinical and genetic study of a family with hereditary essential myoclonus]
V Gualandri1, A Montagnani, L Bevilacqua
1Université de Milan, Faculté de Médecine et Chirurgie, Chaire de Génétique Humaine, Milano Italie.
Revue Neurologique
|January 1, 1987
Abstract:
A large family with essential hereditary myoclonus is reported. Symptoms and signs, the age of clinical onset and the evolution are presented. The disease is autosomal dominant with complete penetrance.