Illuminating Fragile X syndrome

rare_diseases_credit_depositphotos

For Fragile X Awareness Month, we explore advances in pharmacological treatments for the condition.

What is Fragile X Syndrome?

It is estimated that one in 4,000 to 7,000 males and one in 8,000 to 11,000 females have been diagnosed with Fragile X syndrome (FXS), a single gene disorder affecting the fragile X mental retardation 1 (FMR1) gene.1 Individuals with this genetic mutation are unable to synthesize the fragile X mental retardation protein (FMRP), which is necessary for normal brain function.2

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Today's issue

Company Spotlight





More Features in Pharmaceutical