What is Fragile X Syndrome (FXS)

4Treatments for Fragile X Syndrome

There is no cure for fragile X syndrome. The main goal of treatment is to help people with this disorder learn social and language skills. This would require support and collaboration from doctors, parents, therapists, and teachers. Many resources and services are available to help children with fragile X syndrome develop properly. Consult your healthcare provider to look for these opportunities. For treating behavior issues, some prescription medications can help. These include selective serotonin reuptake inhibitors, clonidine, guanfacine, or methylphenidate. [7]

Inheritance of Fragile X Syndrome

Fragile X syndrome can be inherited, meaning the gene can be passed down from parents to their children. However, the genetic inheritance of this disorder is relatively abnormal and complicated. It is advisable to consult a genetic expert to determine whether you need genetic testing. This is especially necessary when you have a family history of fragile X syndrome and decide to have a child. The disorder basically follows the patterns of an X-linked dominant disorder, meaning that getting a mutated X chromosome from either the father or the mother would lead to symptoms. Nevertheless, women with an inherited gene would not have this disorder or only show very mild symptoms. On the other hand, men with an inherited X chromosome will almost surely show symptoms as they get this defect gene from the mother. [8]

Related Articles

Angelman Syndrome – Symptoms and Causes

Ailments & Conditions
Angelman syndrome is a genetic condition that causes considerable intellectual and developmental disability, sleep problems, and movement issues. Kids with this disorder tend to have some distinctive symptoms and features. However, it can be hard to diagnose them once...

Causes of Spinal Muscular Atrophy

Ailments & Conditions
Spinal muscular atrophy is a progressive neurodegenerative condition. This rare genetic disease is often triggered by mutations or alterations in the genes that produce proteins required for motor neuron function. There are many forms of spinal muscular atrophy, which...

Klinefelter Syndrome – Facts to Know

Ailments & Conditions
What Is Klinefelter Syndrome? Klinefelter syndrome is a common genetic disorder. It leads to abnormal developments only in males. Currently, the average time to diagnose this condition is in the mid 30s. However, many people still remain undiagnosed during their...

Spinal Muscular Atrophy – Diagnosis & Treatments

Ailments & Conditions
Spinal muscular atrophy is a rare genetic condition that can affect motor neurons in your spinal cord. This leads to weakness or deterioration of the muscles needed for movement. In most cases, symptoms tend to occur at birth or...

Spinal Muscular Atrophy Symptoms

Ailments & Conditions
Spinal muscular atrophy or SMA is a genetic disease. It causes muscles to become emaciated and weak over time. Most cases can be diagnosed in young children or babies. Currently, there is still no cure for the condition. However,...

What is Marfan Syndrome?

Ailments & Conditions
What Is Marfan Syndrome? Marfan syndrome is a genetic connective tissue condition. It would affect the usual development of the body because connective tissue plays a key role in supporting the skeletal structure and other body parts. In addition, the...

What is Prader-Willi Syndrome – 10 Facts You Need to Know

Ailments & Conditions
What Is Prader-Willi Syndrome? Prader-Willi syndrome is a genetic condition that can be passed from parents to their children. It is mostly present at birth, but diagnosis usually does not occur until later stages in life. People with this disorder...

Williams Syndrome – Causes, Symptoms, Diagnosis & Treatment

Ailments & Conditions
Williams syndrome is a genetic condition characterized by many developmental issues. This syndrome is quite rare as it only occurs in approximately 1 in 10,000 people. A genetic link is often present in those with this health issue, but...