Autosomal recessive cerebellar ataxia type 1
id:
autosomal-recessive-cerebellar-ataxia-type-1-275-8227075
title:
Autosomal recessive cerebellar ataxia type 1
text:
Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement. Signs and symptoms of the disorder first appear in early to mid-adulthood. People with this condition initially experience impaired speech (dysarthria), problems with coordination and balance (ataxia), or both. They may also have difficulty with movements that involve judging distance or scale (dysmetria). Other features of ARCA1 include abnormal eye movements (nystagmus) and
brand slug:
wiki
category slug:
encyclopedia
description:
Hereditary ataxia that has material basis in autosomal recessive inheritance
original url:
https://en.wikipedia.org/wiki/Autosomal_recessive_cerebellar_ataxia_type_1
date created:
date modified:
2023-08-28T18:43:09Z
main entity:
{"identifier":"Q55345810","url":"https://www.wikidata.org/entity/Q55345810"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/1/1a/Blausen_0115_BrainStructures.png","width":1600,"height":1429}
fields total:
13
integrity:
15