What type of disorder is fragile x

Local public school systems can provide services and support for children age 3 years and older. Children can access some services even if they do not attend public school. States have created parent centers. These centers help families learn how and where to have their children evaluated and how to find services. Having support and community resources can help increase confidence in managing FXS, enhance quality of life, and assist in meeting the needs of all family members.

It might be helpful for parents of children with FXS to talk with one another. One parent might have learned how to address some of the same concerns another parent has. Often, parents of children with special needs can give advice about good resources for these children. CDC is working to learn more about the natural history of fragile X so that better approaches to intervention can be developed.

The ORDR website provides information about National Institutes of Health-sponsored biomedical research, scientific conferences, and rare and genetic diseases. Skip directly to site content Skip directly to page options Skip directly to A-Z link. Section Navigation. Facebook Twitter LinkedIn Syndicate. What is Fragile X Syndrome? Minus Related Pages. Signs and Symptoms Signs that a child might have FXS include: Developmental delays not sitting, walking, or talking at the same time as other children the same age ; Learning disabilities trouble learning new skills ; and Social and behavior problems such as not making eye contact, anxiety, trouble paying attention, hand flapping, acting and speaking without thinking, and being very active.

The project is a collaborative effort of the German Society of Anesthesiology and Intensive Care, Orphanet, the European Society of Pediatric Anesthesia, anesthetists and rare disease experts with the aim to contribute to patient safety. Prognosis Prognosis. Life expectancy for people with fragile X syndrome is generally normal. Many affected people participate in an active lifestyle and have good health. Regular medical checkups and awareness of increased health risks may improve the outlook for affected people.

Find a Specialist Find a Specialist. Healthcare Resources To find a medical professional who specializes in genetics, you can ask your doctor for a referral or you can search for one yourself. You can also learn more about genetic consultations from MedlinePlus Genetics. Related Diseases Related Diseases.

Conditions with similar signs and symptoms from Orphanet. The differential diagnosis includes other X-linked intellectual deficiencies, Sotos syndrome, microdeletion syndromes e.

Visit the Orphanet disease page for more information. Research Research. Clinical Research Resources ClinicalTrials. Click on the link to go to ClinicalTrials. Please note: Studies listed on the ClinicalTrials. We strongly recommend that you talk with a trusted healthcare provider before choosing to participate in any clinical study. 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. Look through the list to find study opportunities near you. Patient Registry A registry supports research by collecting of information about patients that share something in common, such as being diagnosed with Fragile X syndrome. The type of data collected can vary from registry to registry and is based on the goals and purpose of that registry. Some registries collect contact information while others collect more detailed medical information.

Learn more about registries. Organizations Organizations. Organizations Supporting this Disease. Organizations Providing General Support.

Do you know of an organization? Living With Living With. Their Web site offers general and condition-specific education resources to help teachers and parents better understand the needs of students who have genetic conditions.

Learn More Learn More. MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic. This website is maintained by the National Library of Medicine.

The Merck Manuals Online Medical Library provides information on this condition for patients and caregivers. NHGRI is part of the National Institutes of Health and supports research on the structure and function of the human genome and its role in health and disease. NORD is a patient advocacy organization for individuals with rare diseases and the organizations that serve them. In-Depth Information 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.

Medscape provides information on this topic. You may need to register to view the medical textbook, but registration is free. The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health.

Visit the website to explore the biology of this condition. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists journal articles that discuss Fragile X syndrome.

Click on the link to view a sample search on this topic. Submit a new question If a child might have had this disorder and was never diagnosed, how does it affect him or her in adulthood? See answer Are individuals with Fragile X syndrome at a higher risk for fractures than individuals without Fragile X?

See answer Have a question? References References. Fragile X syndrome. Genetics Home Reference. FMR1-Related Disorders. The National Fragile X Foundation. Fragile X Research Foundation of Canada. Do you know of a review article? Share this content:. Close Copy Link. You May Be Interested In. How to Find a Disease Specialist.

Tips for the Undiagnosed. Support for Patients and Families. Tips for Finding Financial Aid. Help with Travel Costs. How to Get Involved in Research. Section Navigation. Facebook Twitter LinkedIn Syndicate. Coronavirus Disease Find information and resources for people with developmental and behavioral disabilities. Minus Related Pages. What is Fragile X Syndrome? Associated Disorders.

Related Concerns.