Autosomal Recessive Cerebellar Ataxia Type 1

Summarized by Plex Health
Last Updated: 02 May 2022

Autosomal recessive cerebellar ataxia type 1 is a condition identified by progressive troubles with movement because of a loss of nerve cells in the part of the brain that collaborates movement. Signs and symptoms of the disorder first appear in very early to mid-adulthood. People with this problem initially experience impaired speech, troubles with coordination and equilibrium, or both. Other features of ARCA1 include abnormal eye movements and problems following the activities of things with the eyes.

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions

** If you believe that content on the Plex is summarised improperly, please, contact us, and we will get rid of it quickly; please, send an email with a brief explanation.

*** If you want us to remove all links leading to your domain from Plex.page and never use your website as a source of the "Online Knowledge", please contact us using a corporate email and we will remove everything in 10 business days.

logo

Plex Page is a Biology & Health Sciences "Online Knowledge Base," where a machine summarizes all the summaries.