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NEWS

Fragile X Society - India > News
  • July 24, 2017

I AM HIS SISTER AND HE LOVES ME ONLY FOR THAT

On Fragile X Awareness Day, Avanti Balachander,18 shares her...

  • February 18, 2017

‘Nothing can be done’ in genetic Fragile X Syndrome a myth

The absence of clinical medicine to treat Fragile X...

  • February 2, 2017

Pediatricians to spread awareness about Fragile X Syndrome

The Indian Academy of Pediatrics (IAP) is joining hands...

  • July 15, 2015

Genetic condition more widespread than thought

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About Us

The Fragile X Society is based in Mumbai, India, and has successfully created a network all over the country with parents and eminent doctors. The society promotes public and professional awareness.

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Members of International Fragile X Alliance

Our News

  • I AM HIS SISTER AND HE LOVES ME ONLY FOR THAT
  • ‘Nothing can be done’ in genetic Fragile X Syndrome a myth
  • Pediatricians to spread awareness about Fragile X Syndrome
  • Genetic condition more widespread than thought
  • Launch of India’s first Fragile X Clinic inaugurated in city last week

Contact Info

  • +91 9820199092 | +91 8433853448 | +91 2266642151
  • shalini@fragilex.in | ami@fragilex.in | fragilexindia@yahoo.com

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  • About Fragile X
  • Newly Diagnosed
  • Personal Stories
  • Treatment
  • Testing
  • Regional Representatives
  • News
  • Events
  • About Us
  • About Fragile X
  • Living with Fragile X
    • NEWLY DIAGNOSED
    • Treatment
    • Personal Stories
  • Testing
  • Get Help
    • Regional Representatives
  • News and Events
    • News
    • Events
  • About Us