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Inherited Retinal Diseases (IRDs)

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January 30, 2025

Why in News?

According to a recent study, there is a higher prevalence of Inherited Retinal Diseases (IRDs) situation in India.

  • IRDs – It is a genetic disorder, a change or a variant, in one or more genes that contribute to proper retinal function.
  • Genetic mutations – It stems from mutations in more than 300 genes responsible for the function of the retina, the light-sensitive tissue at the back of the eye.
  • It varies significantly across different communities, and it is difficult to identify common mutations.
  • Impacts – It affects the gene’s ability to do its job properly.
  • The mistake gene doesn’t make a protein and cells in the retina degenerate and cause vision loss.
  • Vulnerables It affects individuals of all ages.

According to the World Health Organization (WHO), more than 2.2 billion people worldwide experience some form of vision impairment.

  • Causes – Lose sight shortly after birth
    • Gradual deterioration over time
    • Progressive vision loss
    • Often resulting in blindness.
  • Treatment - Gene therapy – It is for blindness caused by mutations in the RPE65 genes and treat various inherited eye disorders.
  • RNA-based therapies – To restore protein production in retinal cells without altering the underlying DNA.
  • Treat retinal degenerative diseases caused by single-point mutations.

Studies have revealed significantly higher prevalence, with 1 in 372 individuals in rural South India, 1 in 930 in urban South India, and 1 in 750 in rural Central India affected by these conditions.

References

  1. The Hindu| IRDs Treatment & Precision Therapeutics
  2. Prevent Blindness| Inherited Retinal Diseases (IRDs)
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