Fragile X Clinic

What you should know about Fragile X syndrome:

• FXS is a common inherited cause of neurodevelopmental diagnoses such as intellectual disability, autism spectrum disorder and developmental delay.
  The diagnosis is confirmed through genetic testing called Fragile X DNA analysis.
• FXS affects males and females of all ethnic and socioeconomic backgrounds.
• People with FXS may show a wide range of symptoms, including intellectual disability or learning challenges, behavioral differences such as autism spectrum disorder, attention deficits, anxiety, physical differences and seizures.  
• Targeted pharmaceuticals, intervention strategies and support services can maximize potential in children and adults with FXS.
• Family members of people with Fragile X syndrome may be affected by a variety of gene-related symptoms, including infertility and neurological symptoms such as tremor and loss of coordination or balance (ataxia).

Why choose Geisinger’s Fragile X Clinic?

Geisinger DevMed organizes on average 4 Fragile X Clinics each year. During FXS Clinic days, families can speak with providers from a variety of fields including:

• Neurodevelopmental pediatrics
• Genetics and genomic medicine
• Psychology
• Speech-language pathology
• Behavioral health

This multidisciplinary approach allows us to offer unique and practical services for people with FXS. 

Build your FXS community 

DevMed’s Fragile X Clinic also provides families the opportunity to connect with other families with a child with FXS. Families have stated that they value this opportunity to share resources, build their community and interact with children of all ages with FXS.

Get help where you are, from experts who understand

Our team of specialists is available to provide local and long-distance consultations to help schools, agencies and families address the complex needs of children with Fragile X syndrome across the lifespan.

Participate in research

Geisinger is a member of the international Fragile X Clinical and Research Consortium. That means:

• We are committed to continued learning about Fragile X syndrome through literature, community news and other resources. 
• Research collaborations with organizations such as the National Fragile X Foundation allow us to contribute to increased understanding around Fragile X syndrome. 

To learn more about research opportunities, ask your provider for information during your appointment. 

Resources

• The National Fragile X Foundation | Fragile X syndrome
• DevMed-approved resources for children with special developmental needs