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pro vyhledávání: '"N. N. Aldawoodi"'
Publikováno v:
Case Reports in Anesthesiology, Vol 2019 (2019)
Spinocerebellar ataxia 3 (SCA3), also known as Machado–Joseph disease (MJD) is an autosomal dominant, progressive neurodegenerative disorder. Patients present with cerebellar ataxia, dystonia, rigidity, and neuropathy that worsen with time. On a mo
Externí odkaz:
https://doaj.org/article/6f664f8ccccf480898c0e15ccbbc26e9
Publikováno v:
Case Reports in Anesthesiology
Case Reports in Anesthesiology, Vol 2019 (2019)
Case Reports in Anesthesiology, Vol 2019 (2019)
Spinocerebellar ataxia 3 (SCA3), also known as Machado–Joseph disease (MJD) is an autosomal dominant, progressive neurodegenerative disorder. Patients present with cerebellar ataxia, dystonia, rigidity, and neuropathy that worsen with time. On a mo