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Familial Progressive Myoclonic Epilepsy (Unverricht-Lundborg syndrome in five families from the Valais canton)1,2

Published online by Cambridge University Press:  01 August 2014

Eduardo Rallo
Eduardo Rallo*
Affiliation:
Institut de Génétique Medicale de l'Université de Genève
*
Institut de Génétique Médicale de l'Université, Chemin Thury 8, 2106 Genève (Suisse)

Summary

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After a historical review of the problem of progressive myoclonic epilepsy, the author makes a detailed clinical and genetic description of 5 families from the Valais canton, affected with the disease. The metabolic disturbances observed in these cases (urinary elimination of mucopolysaccharides) are given particular attention. The author further discusses the various classifications of myoclonic epilepsy which were established on the basis of clinical symptomatology, electroencephalographic tracings, pathological anatomy and biochemical findings.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 18 , Issue 3 , July 1969 , pp. 231 - 270
Copyright
Copyright © The International Society for Twin Studies 1969

Footnotes

1

Travail subventionné par le Fonds National Suisse de la Recherche Scientifique (Crédit No. 4408) et par le Public Health Service, Bethesda, Md., USA (NB 04590-05).

2

Ce travail est dédié en hommage sincère au Prof. D. Klein pour son soixantième anniversaire.

References

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