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  Published Paper Details:

  Paper Title

  Authors

  Mrs. K.PUNITHA

  Keywords

Key word: Syndrome, Neuropathy, Mutations, Chromosome, Fungiform Papillae

  Abstract


ABSTRACT: Riley-Day syndrome is a hereditary sensory and autonomic neuropathy type III (HASAN) resulting insensitivity to pain, inability to produce tears, poor growth and labile blood pressure. It is caused by mutations in IKBKAP gene on chromosome 9. On clinical diagnosis no fungiform papillae on the tongue, there is deep tendon reflexes and lack of an axon flare, genetic test denotes presence of chromosome 9. Treatment of Riley-Day syndrome is preventative, symptomatic, and supportive. Medicines are used to control vomiting, eye dryness, and blood pressure. Central nervous system degeneration have a poor long term prognosis.

  IJCRT's Publication Details

  Unique Identification Number - IJCRT2104020

  Paper ID - 205134

  Page Number(s) - 132-135

  Pubished in - Volume 9 | Issue 4 | April 2021

  DOI (Digital Object Identifier) -   

  Publisher Name - IJCRT | www.ijcrt.org | ISSN : 2320-2882

  E-ISSN Number - 2320-2882

  Cite this article

  Mrs. K.PUNITHA,   "RILEY-DAY SYNDROME", International Journal of Creative Research Thoughts (IJCRT), ISSN:2320-2882, Volume.9, Issue 4, pp.132-135, April 2021, Available at :http://www.ijcrt.org/papers/IJCRT2104020.pdf

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ISSN: 2320-2882
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ISSN and 7.97 Impact Factor Details


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ISSN
ISSN: 2320-2882
Impact Factor: 7.97 and ISSN APPROVED
Journal Starting Year (ESTD) : 2013
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