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Ataxia with Vitamin E Deficiency
What is Ataxia with Vitamin E Deficiency?
Ataxia with vitamin E deficiency (AVED) is an inherited disorder that affects the body's ability to utilize vitamin E. This condition will lead to difficulty coordinating movements, clumsiness of the hands, loss of reflexes in legs and sensation in extremities, and blurred vision. Most affected individual start to experience problems with movement between the age of 4 and 18 years, which will worsen with age. In some cases, the cognitive ability of the affected individuals may decline. If untreated, affected individuals become wheelchair bound between ages of 11 and 50 years as a result of lack of muscle control and/or leg weakness. The life expectancy of individuals with AVED may be shortened. AVED can be treated with vitamin E supplementation, which can reverse some symptoms if treatment is initiated during the progress of the disease, or prevent symptoms altogether if initiated before symptoms appear. AVED is caused by pathogenic variants in the TTPA gene.
How is Ataxia with Vitamin E Deficiency inherited?
AVED is inherited in an autosomal recessive manner. This type of inheritance requires the presence of two copies of a pathogenic variant in the gene for a person to have the genetic disease. Both parents must be carriers of a pathogenic variant in the gene in order to be at risk to have an affected child. The child must inherit a pathogenic variant from each carrier parent in order to be affected. There is a 1 in 4 chance that a baby will inherit two mutated copies of the gene and be affected when both parents are carriers.
What does it mean to be a carrier?
There are generally no signs or symptoms associated with being a carrier for AVED. However, the risk to have a child affected with AVED is increased. Testing of reproductive partners is recommended for carriers of AVED.
How common is Ataxia with Vitamin E Deficiency?
What is analysed?
|Ethnicity||Detection Rate||Carrier Frequency|
|General Population||> 99%||1 in 500|