These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: A case of spinocerebellar ataxia type 6 mimicking olivopontocerebellar atrophy.
    Author: Nakagawa N, Katayama T, Makita Y, Kuroda K, Aizawa H, Kikuchi K.
    Journal: Neuroradiology; 1999 Jul; 41(7):501-3. PubMed ID: 10450843.
    Abstract:
    Spinocerebellar ataxia type 6 (SCA6) is an autosomal dominant, slowly progressive cerebellar ataxia without multisystem involvement. We report a 57-year-old woman with genetically confirmed SCA6 who showed clinical features of olivopontocerebellar atrophy. Conventional T2-weighted and FLAIR MRI demonstrated high signal in the middle cerebellar peduncles, in addition to mild atrophy of the pons and cerebellum.
    [Abstract] [Full Text] [Related] [New Search]