SYNE1;related autosomal recessive cerebellar ataxia

SYNE1-Related Autosomal Recessive Cerebellar Ataxia

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SYNE1
SYNE1-related autosomal recessive cerebellar ataxia (also known as autosomal recessive cerebellar ataxia type 1, or ARCA1) is characterized by onset of cerebellar ataxia and/or dysarthria at a mean age of 31 years (range 17-46 years). Over time, all affected individuals develop significant dysarthria and ataxia. Other associated features can include dysmetria, brisk lower-extremity tendon reflexes, and minor abnormalities in ocular saccades and pursuit. Disease progression is slow, resulting in moderate disability. Life expectancy appears to be normal. ARCA1 has not been observed outside of Quebec, Canada.

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News and Updates
SYNE1 Gene Database
Posted on 2007-07-30 12:12:29
The purpose of this website is to create a new database for the SYNE1 Gene mostly reported in the province of Quebec, Canada.

This project is supported by the RMGA (Réseau Médecine Génétique Appliqué).

http://www.medgen.mcgill.ca/syne1/


What's New? Administrator Page
Posted on 2007-07-30 12:09:58
Administrator who have a login Username and Password can now create, edit and delete the What's New? section of this web site.

The What's New? section will inform users of recent news in the SYNE1 development, show the development of this web site and post relative information about the world of Genetics in general.

http://www.medgen.mcgill.ca/syne1/Admin.php


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