The World Fragile X Awareness Day is marked on 22 July every year to celebrate families impacted by Fragile X and highlight the progress of research to find a cure. On this day, communities around the world come together to shine a light on Fragile X, by illuminating monuments and landmarks globally. World Fragile X Day celebrates families impacted by Fragile X and highlights advancements of research to find effective treatments and ultimately a cure.
Fragile X or Martin-Bell Syndrome
- Fragile X syndrome (FXS) is an inherited genetic disease passed down from parents to children that causes intellectual and developmental disabilities.
- FXS is the most common hereditary cause of mental disability in boys. It affects 1 in 4,000 boys.
- It’s less common in girls, affecting about 1 in every 8,000. Boys usually have more severe symptoms than girls.
- People with FXS usually experience a range of developmental and learning problems.
- The disease is a chronic or lifelong condition. Only some people with FXS are able to live independently.
Causes
- FXS is caused by a defect in the FMR1 gene located on the X chromosome.
- The FMR1 (Fragile X Mental Retardation 1 gene) gene is located on the X chromosome in humans. It is responsible for producing a protein called FMRP (Fragile X Mental Retardation Protein), which plays a crucial role in normal brain development and function.
Risks
- Women who are carriers are at an increased risk for premature menopause, or menopause that starts before the age of 40.
- Men who are carriers are at increased risk for a condition known as Fragile X Tremor Ataxia Syndrome (FXTAS).
- The disorder results in progressive cerebellar ataxia, action tremor, Parkinsonism and cognitive decline.
It also can lead to difficulty with balance and walking. Male carriers may also be at an increased risk for Dementia.
Linked with Inheritance
- Women who carry Fragile X have a 50% chance of passing the mutated gene to each of her children. If she passes the affected gene, her children will either be carriers, or they will have Fragile X syndrome.
- Men who carry Fragile X will pass the premutation to all their daughters but none of their sons. These daughters are carriers, but they do not have Fragile X syndrome.