Portuguese-Azorean disease

Ma·cha·do-Jo·seph disease

(mă-sha'dō jō'seph), [MIM*109150]
a rare form of hereditary ataxia, characterized by onset in early adult life of progressive, spinocerebellar and extrapyramidal disease with external ophthalmoplegia, rigidity dystonia symptoms, and, often, peripheral amyotrophy; found predominantly in people of Azorean ancestry; autosomal dominant inheritance, caused by a trinucleotide repeat expansion mutation in the Machado-Joseph gene (MJD1) on 14q.
[Surnames of two families studied in major descriptions of the disease.]
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