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Article
February 1986

Machado-Joseph-Azorean Disease in India

Author Affiliations

From the Neuroepidemiology Department, Bombay (India) Hospital Medical Research Center (Drs N. E. Bharucha and E. P. Bharucha), and the Department of Neurology, K. E. M. Hospital and Seth G. S. Medical College, Bombay, India (Drs N. E. Bharucha, E. P. Bharucha, and Bhabha).

Arch Neurol. 1986;43(2):142-144. doi:10.1001/archneur.1986.00520020036014
Abstract

• Machado-Joseph-Azorean (MJA) disease is an autosomal-dominant multisystem motor degeneration (with cerebellar ataxia as an important manifestation) that is seen mainly in people of Portuguese descent. Recently, a family in Japan with probable MJA disease has been described. We describe a family with clinical features similar to those of MJA disease; these are the first cases to be described in India. Further pathologic study is necessary to confirm the diagnosis in our cases. Meanwhile, further search for such cases in India should yield interesting genetic clues to the disease.

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