{"id":108360,"date":"2021-05-25T09:49:30","date_gmt":"2021-05-25T09:49:30","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=108360"},"modified":"2021-05-25T09:49:30","modified_gmt":"2021-05-25T09:49:30","slug":"maries-ataxia","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/maries-ataxia\/","title":{"rendered":"Marie&#8217;s ataxia"},"content":{"rendered":"<p>Ataxia is a disorder that involves incoordination of voluntary muscle movements. Marie\u2019s ataxia is a designation for hereditary conditions expressed through dominant genes and characterized by spinocerebellar degeneration. These conditions normally occur in adulthood, although the time of onset varies widely. The clinical features of Marie\u2019s ataxia are heterogeneous within and between families, so diagnosis and classification are difficult.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Ataxia is a disorder that involves incoordination of voluntary muscle movements. Marie\u2019s ataxia is a designation for hereditary conditions expressed through dominant genes and characterized by spinocerebellar degeneration. These conditions normally occur in adulthood, although the time of onset varies widely. The clinical features of Marie\u2019s ataxia are heterogeneous within and between families, so diagnosis [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":["post-108360","post","type-post","status-publish","format-standard","hentry","category-m"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Marie&#039;s ataxia - Definition of Marie&#039;s ataxia<\/title>\n<meta name=\"description\" content=\"Ataxia is a disorder that involves incoordination of voluntary muscle movements. Marie\u2019s ataxia is a designation for hereditary conditions expressed through dominant genes and characterized by spinocerebellar degeneration. These conditions normally occur in adulthood, although the time of onset varies widely. 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