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Diagnostic Tests

Fragile X Syndrome

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Fragile X Syndrome

Also known as Fragile X Syndrome Karyotyping Blood
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What is this test?

Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Usually, males are more severely affected by this disorder than females. Affected individuals usually have delayed development of speech and language by age 2. Most males with fragile X syndrome have mild to moderate intellectual disability, while about one-third of affected females are intellectually disabled. Children with fragile X syndrome may also have anxiety and hyperactive behavior such as fidgeting or impulsive actions. They may have attention deficit disorder (ADD), which includes an impaired ability to maintain attention and difficulty focusing on specific tasks. Fragile X syndrome (FXS) is an inherited genetic disease passed down from parents to children that causes intellectual and developmental disabilities. It

Also known as Fragile X Syndrome Karyotyping.

Test Preparation

No special preparation is needed for Fragile X Syndrome. Inform your doctor if you are on any medications or have any underlying medical conditions or allergies before undergoing Fragile X Syndrome. Your doctor depending on your condition will give specific instructions.

Understanding your test results

GenderAge groupsValue
UNISEXAll age groupsExpansion of CGG trinucleotide repeat sequence is seen in positive cases
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