CJG Blog

Center for Jewish Genetics blog

Fragile X Awareness Month

 Permanent link

ChromosomepuxxleBy: Lilli Arbetter

July is Fragile X Awareness Month, which is devoted to bringing attention to Fragile X Syndrome (FXS). FXS is a disease that leads to intellectual disability (the leading genetic cause of autism spectrum disorder) and is prevalent in the Ashkenazi Jewish population.  

What causes FXS? The fragile X mental retardation 1 gene (FMR1) makes a protein called the fragile X mental retardation protein (FMRP), which is needed for typical brain development. Those who have FXS do not make this protein. In the FMR1 gene, there is a section of the DNA pattern, CGG, that is repeated many times. A small number of repeats (5 to 44) is normal; however, the following occurs as the number of repeats increase: 

  • 45 to 54 repeats: Those within this range of repeats are called intermediate carriers and do not have FXS. Their offspring are not at risk for FXS, but future generations may be at risk. 
  • 55 to 200 repeats: Those within this range of repeats are called premutation carriers. They do not have FXS but have a premutation. Premutation carriers have an increased risk for adult-onset symptoms, such as tremor-ataxia syndrome, premature ovarian insufficiency, and neuropsychiatric disorders. A woman within this range of repeats has a 50% chance of passing the premutation or full mutation on to their daughter or son. A man within this range will have a daughter with a premutation, but his son will not be affected. 
  • 200+ repeats: Those with 200+ repeats have a full mutation and therefore, have FXS.  

Children of any sex can have FXS and its associated symptoms; however, the symptoms are often more severe in males. Since females have two X chromosomes, the working copy of the FMR1 gene can compensate for the inherited non-working FMR1 gene copy. This means that although they may have FXS, their symptoms are often not as severe. However, males only have one X chromosome, so if they inherit a damaged copy, they do not have another gene to compensate for the mutated one and will have more severe symptoms.  

For men who are carriers of FXS, the disorder tends to skip generations. When a father passes the premutation on to his daughter, she can become a carrier and her children can inherit the disorder. Unlike men, for women who are carriers, their mutation can expand and get bigger with each generation.  

Anyone considering FXS testing should consult with a genetic counselor. A diagnosis of FXS can provide an explanation for a child’s behavioral problems and allow a family to obtain treatment for the child to reach their full potential. Although there is no cure, there are options such as medication, therapy, and other treatment/support that a genetic counselor can help advise. 

Resources: 

Baby1

Affordable, Accessible Genetic Screening in Illinois

Our affordable, accessible carrier screening program uses advanced technology to provide comprehensive screening for Jewish and interfaith couples. Visit our Get Screened page to learn more and register.

CJG-Whats-In-Your-Genes

Do You Know What's In Your Genes?

What is the most valuable gift you can give to your family? The gift of good health! There are many health conditions that run in families. Knowing your family health history can alert you to the potential risk for a variety of genetic disorders . Talk to your relatives for warning signs and assess your risk for hereditary cancers.

Did you know: Ashkenazi Jews are 10 TIMES more likely to have BRCA mutations, which significantly increases lifetime risks for hereditary cancers, so what does this heightened risk mean for you? Click here to learn more .