A BRIEF REVIEW ON FREDREICH ATAXIA DISEASE
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.
"A BRIEF REVIEW ON FREDREICH ATAXIA DISEASE", IJNRD - INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT (www.IJNRD.org), ISSN:2456-4184, Vol.8, Issue 3, page no.a840-a847, March-2023, Available :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: 000118840
Research Area: Pharmacy
Country: Pune, Maharashtra, India
ISSN: 2456-4184 | IMPACT FACTOR: 8.76 Calculated By Google Scholar | ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.76 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator
Publisher: IJNRD (IJ Publication) Janvi Wave
