Abstract
The Andermann syndrome is a familial disease that was initially described in the Saguenay-Lake St-Jean area in Quebec. A few cases have now been reported outside of Quebec (see Andermann and Andermann, this volume). Agenesis of the corpus callosum is usually, but not invariably, part of the syndrome. We have had the opportunity of studying the brains of two patients suffering from Andermann’s Syndrome, as well as six sural nerve biopsies.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Larbrisseau, A., Vanasse, M., Brochu, P., and Jasmin, G., 1984, The Andermann Syndrome: Agenesis of the corpus callosum associated with mental retardation and progressive sensorimotor neuronopathy, Can. J. Neurol. Sci. 11: 257–261.
Love, S. and Cruz-Höfling, M.A., 1986, Acute swelling of nodes of Ranvier caused by venoms which slow inactivation of sodium channels, Acta Neuropathol. 70: 1–9.
Mathieu, J., Bedard, F., Prévost, C., and Langevin, P., 1990, Neuropathie sensitivo-motrice héréditaire avec ou sans agénésie du corps calleux: Etude radiologique et clinique de 64 cas, Can. J. Neurol. Sci. 17: 103–108.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1994 Plenum Press, New York
About this chapter
Cite this chapter
Carpenter, S. (1994). The Pathology of the Andermann Syndrome. In: Lassonde, M., Jeeves, M.A. (eds) Callosal Agenesis. Advances in Behavioral Biology, vol 42. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-0487-6_4
Download citation
DOI: https://doi.org/10.1007/978-1-4613-0487-6_4
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4612-7592-3
Online ISBN: 978-1-4613-0487-6
eBook Packages: Springer Book Archive