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Book Sca7 Spinocerebellar Ataxia Type 7 , Cag Repeats Test in Bangalore-urban

Spinocerebellar Ataxia Type 7 (SCA7) is a rare inherited neurodegenerative disorder resulting from the expansion of CAG repeats in the ATXN7 gene. This expansion leads to the production of abnormal ataxin-7 protein, resulting in progressive impairment of movement coordination, vision loss, and other neurological symptoms. Diagnostic testing for SCA7 involves analyzing the length of CAG repeats in the ATXN7 gene, aiding in confirming the diagnosis, predicting disease severity, and providing genetic counseling for individuals and their families.

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Spinocerebellar Ataxia Type 7 (SCA7) is a rare inherited neurodegenerative disorder resulting from the expansion of CAG repeats in the ATXN7 gene. This expansion leads to the production of abnormal ataxin-7 protein, resulting in progressive impairment of movement coordination, vision loss, and other neurological symptoms. Diagnostic testing for SCA7 involves analyzing the length of CAG repeats in the ATXN7 gene, aiding in confirming the diagnosis, predicting disease severity, and providing genetic counseling for individuals and their families.

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312 hours
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Frequently Asked Questions about Sca7 Spinocerebellar Ataxia Type 7 , Cag Repeats Test in Bangalore Urban