In people with SCA3, the CAG segment is repeated more than 50 times. Most people have fewer than 31 CAG repeats. Normally, the CAG segment is repeated 12 to 43 times within the gene.
This segment is made up of a series of three DNA building blocks (cytosine, adenine, and guanine) that appear multiple times in a row. The ATXN3 gene mutations that cause SCA3 involve a DNA segment known as a CAG trinucleotide repeat. Researchers believe that ataxin-3 also may be involved in regulating the first stage of protein production ( transcription ). Ataxin-3 removes the ubiquitin from these unwanted proteins just before they are degraded so that the ubiquitin can be used again. The molecule ubiquitin is attached (bound) to unneeded proteins, which tags them to be broken down (degraded) within cells. Ataxin-3 is involved in a mechanism called the ubiquitin-proteasome system that destroys and gets rid of excess or damaged proteins. The ATXN3 gene provides instructions for making an enzyme called ataxin-3, which is found in cells throughout the body.
They usually survive 10 to 20 years after symptoms first appear. People with SCA3 eventually require wheelchair assistance. Signs and symptoms of the disorder typically begin in mid-adulthood but can appear anytime from childhood to late adulthood. Individuals with SCA3 may have problems with memory, planning, and problem solving. Over time, individuals with SCA3 may develop loss of sensation and weakness in the limbs (peripheral neuropathy), muscle cramps, muscle twitches (fasciculations), and swallowing difficulties. These sleep disorders tend to leave affected individuals feeling tired during the day. REM sleep behavior disorder is a condition in which the muscles are active during the dream (REM) stage of sleep, so an affected person often acts out his or her dreams. Restless leg syndrome is a condition characterized by numbness or tingling in the legs accompanied by an urge to move the legs to stop the sensations. People with this condition may experience sleep disorders such as restless leg syndrome or REM sleep behavior disorder. Other early signs and symptoms of SCA3 include speech difficulties, uncontrolled muscle tensing (dystonia), muscle stiffness (spasticity), rigidity, tremors, bulging eyes, and double vision. People with this condition initially experience problems with coordination and balance (ataxia).
Marketing Science Consulting Group, Inc.Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by progressive problems with movement.Dansk Deutsch English Español Français Italiano Magyar Nederlands Norsk Polski Português Suomi Svenska Čeština Русский 日本語 简体中文 한국어 Настройки файлов cookie