Machado-Joseph Disease

Authors

  • J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-10-6-11

Keywords:

Spinocerebellar Ataxia 3, Machado-Joseph Disease, Autosomal Dominant Cerebellar Ataxia

Abstract

The frequency, and clinical, molecular, and neuropathological features of spinocerebellar ataxia 3 (SCA3) and Machado-Joseph disease (MJD) in 125 autosomal dominant cerebellar ataxia (ADCA) families were analyzed at the Service de Neuropathologie, Hopital de la Salpetriere, Paris, and Service de Neurologie, Hopital de Haut Leveque, Pessac, France; and Service de Neurologie, Hopital des Specialites, Rabat, Morocco.

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Published

1996-06-01

Issue

Vol 10, No 06 | Jun 1996

Section

Ataxic Disorders

License

Copyright (c) 1996 The Author(s)

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