"For the first time, we have hope that medicines are within sight that will allow many individuals with fragile X syndrome and autism, who have severe social impairments, to be able to function and interact with others in society," said Robert Miller, Executive Director of the National Fragile X Foundation.
While autism is the more commonly known of the two conditions, fragile X syndrome is the most common known genetic cause of autism and autism spectrum disorders. It is also the most common cause of inherited intellectual disability and can cause learning and behavioral disorders that can range from mild to severe. New scientific research has further established the interconnectivity between these two conditions.
The enthusiasm for these new discoveries into the genetic causes of autism is tempered by the reality that federal budget constraints may jeopardize the significant scientific gains made. Hundreds of advocates, including researchers and families of individuals with FXS and autism, will be in Washington on March 5 and 6 to help raise public and Congressional awareness of the break-through research's potential for treatment.
"With actual treatments for key symptoms of autism and fragile X syndrome in the testing phase, the impact of recent scientific discoveries cannot be underestimated--and should not be starved of support just as they are coming to reality," Miller said.
The National Fragile X Foundation, founded in 1984, is a 501(c)(3) nonprofit organization that provides informational, referral and emotional support; educational and awareness materials and activities; support for research including the translation of science into new and improved treatments; and legislative advocacy. More information is available at www.fragilex.org.
Web Site: http://www.fragilex.org
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