Sentinel Node Biopsy and Lumpectomy in a Patient with Machado–Joseph Disease

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 molecular level, it occurs due to a CAG trinucleotide...

Full description

Bibliographic Details
Main Authors: N. N. Aldawoodi, A. R. Escher Jr., A. Padalia, D. Padalia
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Case Reports in Anesthesiology
Online Access:http://dx.doi.org/10.1155/2019/2309598