Spinocerebellar ataxia: Revision history

Jump to navigation Jump to search

Diff selection: Mark the radio buttons of the revisions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with latest revision, (prev) = difference with preceding revision, m = minor edit.

11 December 2023

23 March 2023

26 December 2022

  • curprev 03:5803:58, 26 December 2022Oldver>Mehrdad 808 bytes +808 Created page with "=== Clinic === * '''SCA''' is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. * SCA is hereditary, progressive, degenerative, and often fatal. * Hereditary ataxias can be inherited in an autosomal dominant, autosomal recessive, or X-linked manner. === Signs / Symptoms === * Slowly progressive incoordination of gait * Poor coordination of hands, * Poor coordination of spe..."