A BRIEF REVIEW ON FREDREICH ATAXIA DISEASE

Registration ID: IJNRD_188360

Published ID: IJNRD2303091

DOI: Click Here to Get

ROHIT RAGHUNATH NANDE , HINGNE L.D , BAGWAN LATIF RASHID

Immunity, alleles ,mutation

There Friedreich ataxia, an autosomal passive neurodegenerative infection, is the most well-known of the acquired ataxias. The new revelation of the quality that is transformed in this condition, FRDA, has prompted quick advances in the comprehension of the pathogenesis of Friedreich ataxia. Changes in the FXN gene trigger the FA problem. The FXN gene possesses chromosome in the chromosome map. Mutations in the FXN gene comprise of four classes of alleles. These incorporate ordinary alleles, alterable typical alleles, complete penetrance alleles, and borderline alleles. Currently, there is no productive treatment for this problem. To slow down FA, hereditary methodology can be utilized. The methodology might include genetic counselling and utilization of quality treatment. In genetic counselling, in the event that the two guardians are transporters, a kid has a 25 % FA. To distinguish individuals with transporter, amniocentesis can be utilized for instance.

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ROHIT RAGHUNATH NANDE, HINGNE L.D , & BAGWAN LATIF RASHID (March-2023). A BRIEF REVIEW ON FREDREICH ATAXIA DISEASE. INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT, 8(3), a840-a847. https://ijnrd.org/papers/IJNRD2303091.pdf

Volume 8 Issue 3, March-2023

Pages : a840-a847

Paper Reg. ID: IJNRD_188360

Published Paper Id: IJNRD2303091

Downloads: 000121983

Research Area: Pharmacy

Country: Pune, Maharashtra, India

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