Fragile X syndrome
Other Names for this Disease
- Fra(X) syndrome
- FraX syndrome
- FRAXA syndrome
- Marker X syndrome
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There is no specific treatment available for fragile X syndrome. Management of this condition is generally supportive and may include:
- recognizing the need for special education and avoiding excessive stimulation, which may help with behavioral problems
- early educational intervention and special education that is tailored to specific learning difficulties; small class size, individual attention and avoidance of sudden change is often needed
- medications for behavioral issues that affect social interaction
- routine medical management of strabismus, ear infections, reflux, seizures, mitral valve prolapse, and/or high blood pressure.
Last updated: 1/28/2015
- Robert A Saul and Jack C Tarleton. FMR1-Related Disorders. GeneReviews. April 26, 2012; http://www.ncbi.nlm.nih.gov/books/NBK1384/.
- GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions. Click on the link to view the article on this topic.
- American Academy of Pediatrics Guidelines: Health Supervision for Children with Fragile X Pediatrics 2011; 127: 994-1006.
- ClinicalTrials.gov lists trials that are studying or have studied Fragile X syndrome. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
- NIH Issues Research Plan on Fragile X Syndrome and Associated Disorders. NIH News. July 20, 2009.
- The National Fragile X Foundation provides a state by state list of clinical trials involving fragile X-associated disorders. Click on National Fragile X Foundation to view the list.
- The FRAXA Research Foundation lists clinical trials seeking participants. The trials are sorted by sponor and then by state. Look through the list to find study opportunites near you.