Fragile X syndrome
FAQs
- Q1 What is Fragile X syndrome?
- Q2 What are the characteristics of Fragile X syndrome?
- Q3 What causes Fragile X syndrome?
- Q4 How does Fragile X syndrome impact on carers, friends and family?
- Q5 What are NPL-2005 and NPL-2009?
- Q6 Where and when will NPL-2005 and NPL-2009 be made available to patients?
- Q7 Can my child take part in clinical trials for NPL-2005 or NPL-2009?
Q4 How does Fragile X syndrome impact on carers, friends and family?
Fragile X syndrome is a genetically inherited condition. This means that when a child is diagnosed with the condition it often has an impact on the entire family. Transmitted on the X chromosome, Fragile X syndrome can be unknowingly carried by both males and females before manifesting itself further down the family line – so genetic counselling and support is usually essential.
Caring for a Fragile X syndrome child can be very stressful, with large amounts of time needing to be dedicated to the affected individual.