Paper Title
A BRIEF REVIEW ON FREDREICH ATAXIA DISEASE
Article Identifiers
: Authors
Keywords
Immunity, alleles ,mutation
Abstract
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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How To Cite (APA)
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
Issue
Volume 8 Issue 3, March-2023
Pages : a840-a847
Other Publication Details
Paper Reg. ID: IJNRD_188360
Published Paper Id: IJNRD2303091
Downloads: 000122001
Research Area: Pharmacy
Author Type: Indian Author
Country: Pune, Maharashtra, India
Published Paper PDF: https://ijnrd.org/papers/IJNRD2303091.pdf
Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2303091
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