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...

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Detalles Bibliográficos
Autores principales: Aldawoodi, N. N., Escher Jr., A. R., Padalia, A., Padalia, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942782/
https://www.ncbi.nlm.nih.gov/pubmed/31934455
http://dx.doi.org/10.1155/2019/2309598

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942782/
https://www.ncbi.nlm.nih.gov/pubmed/31934455
http://dx.doi.org/10.1155/2019/2309598

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