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In page Ataxia–telangiectasia:

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Ataxia–oculomotor apraxia type 2 (AOA2) is an autosomal recessive disorder also similar to A–T in manifesting increasing problems with coordination and peripheral neuropathy, but oculomotor apraxia is present in only half of the affected individuals. Ocular telangiectasia does not develop. Laboratory abnormalities of AOA2 are like A–T, and unlike AOA1, have an elevated serum AFP level, but like AOA1 and unlike A–T in having normal markers of immune function. Genetic testing of the senataxin gene (SETX) can confirm the diagnosis. There is no enhanced risk for cancer.[citation needed]