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Genetics Alert
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Usher Syndrome: Type IF

  • What is Usher Syndrome: Type IF?

    Usher syndrome type I (USH1) is an inherited disorder that causes hearing loss at birth and progressive vision loss starting in adolescence. The vision loss begins as night blindness in early adolescence followed by a gradual loss of peripheral vision. Development of cataracts may further reduce vision. Children with USH1 also learn to sit and walk at a later age than other children and have balance problems as they grow older. The life expectancy and intellect of individuals with USH1 is not affected. Without help from a cochlear implant, individuals typically do not develop speech. USH1 is caused by pathogenic variants in several genes, including MYO1A, USH1C, CDH23, and PCDH15.

  • How is Usher Syndrome: Type IF inherited?

    Usher syndrome type I 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 USH1. However, the risk to have a child affected with USH1 is increased. Testing of reproductive partners is recommended for carriers of USH1.

  • How common is Usher Syndrome: Type IF?

  • What is analysed?

Ethnicity Detection Rate Carrier Frequency
General Population 63% 1 in 249