Fragile X Syndrome Test Price | Lahalak Platform

Precise genetic analysis to detect mutations causing Fragile X Syndrome, providing clear insights to support cognitive development and healthy growth for children and families.

Prices starts from: 601.92 SAR

Scientific name: Fragile X Syndrome Test

The Fragile X Syndrome test is a genetic test used to detect mutations in the FMR1 gene, which is responsible for Fragile X Syndrome, one of the most common genetic causes of intellectual disability. This test is important in diagnosing the syndrome, as symptoms may appear in childhood, such as speech delays, social communication difficulties, and...

Fragile X Syndrome Test - Fragile X Syndrome Genetic Test
Service type Genetic Test (Blood)
Duration 10-15 minutes
Fasting Fasting is not required
Prices Starting from 601.92 SAR

Included Services

  • Fragile X Test
  • The optimal health guidance based on the result.
  • Personal support services from Lahalak

Medical Service Information

Purpose Test

  • Determining Repeat Numbers: Measures the number of CGG repeats in the FMR1 gene. Normally, the number is less than 45 repeats. If the number is between 55 and 200, it is considered a "premutation" and may increase the risk of the syndrome in future generations. If the number exceeds 200, it indicates the presence of Fragile X syndrome.
  • Syndrome Diagnosis: The test helps confirm the diagnosis of Fragile X syndrome in individuals showing symptoms related to intellectual and behavioral disabilities.
  • Genetic Risk Assessment: Helps determine whether individuals carrying the mutations have a higher risk of passing the syndrome to their children.
  • Providing Additional Information: The test can provide useful insights into the individual’s overall health and guide healthcare and treatment.

Recommended groups

  • Individuals with Developmental Delays: Children showing delays in language, social, or behavioral skills.
  • Individuals with Intellectual Disabilities: People with low intelligence levels or unexplained learning difficulties.
  • Children with a Family History: Children from families with known cases of Fragile X syndrome or mutations in the FMR1 gene.
  • Pregnant Women or Those Planning Pregnancy: Women with a family history of Fragile X syndrome, where it may be necessary to assess the risk of passing the syndrome to future generations.
  • Individuals Showing Syndrome-Related Behaviors: Such as behavioral disorders, anxiety, or social stress.
  • Individuals with Nonspecific Symptoms: Such as poor social communication or repetitive behaviors without a clear cause.

Symptoms indicative

  • Developmental Delays: Delays in language or motor skills compared to peers.
  • Intellectual Disability: Learning difficulties or low intelligence levels that may appear in children.
  • Repetitive Behaviors: Such as repetitive hand movements or excessive focus on a particular object.
  • Social Communication Problems: Difficulties in social interaction or communication, such as poor conversational skills or inability to understand social cues.
  • Behavioral Disorders: Such as excessive anxiety, irritability, or mood swings.
  • Distinctive Appearance: Some individuals with the syndrome may show physical traits such as a long face, large ears, or a narrow high palate.

FAQs

  • What is the purpose of this test? The purpose is to detect mutations in the FMR1 gene to diagnose Fragile X syndrome, which affects intellectual and behavioral development.
  • When is this test recommended? It is recommended when symptoms of developmental delay, intellectual disability, or a family history of the syndrome are present.
  • How is this test performed? The test is conducted by taking a blood sample and analyzing the DNA to detect genetic mutations.
  • Should medications be stopped before the test? Usually, it is not necessary to stop medications, but consult your doctor regarding any medications you are taking.
  • What do the test results mean? The results indicate whether mutations in the FMR1 gene are present, helping determine if the person has Fragile X syndrome.
  • Can the test result be a false positive? Although results are usually accurate, false positives or negatives may occur, so discussing the results with a doctor is important.

Normal Levels

  • Normal: Less than 45 repeats (the person is considered non-carrier of mutations).
  • Premutation: Between 55 and 200 repeats (the person may carry Fragile X, increasing the risk of passing it to future generations, but may not show obvious symptoms).
  • Fragile X Syndrome: More than 200 repeats (indicates the person has Fragile X syndrome and is likely to exhibit related symptoms).

Conditions & Notices

  • The terms and conditions announced on the "Lahalak" medical platform apply.
  • There are no special conditions for the service other than those mentioned.

Medical services you might also like

Factor V Cambridge Mutation Test

Factor V Cambridge Mutation Test

Genetic analysis detecting the Cambridge mutation in Factor V to assess hereditary clotting risks and safeguard your car...

Starting from 147.83 SAR
HLA Cw Typing Test

HLA Cw Typing Test

A precise test measuring HLA-Cw antigens to assess immune function and tissue compatibility, essential for organ transpl...

Starting from 401.27 SAR
BRAF Gene Mutation Test

BRAF Gene Mutation Test

An advanced genetic test to detect BRAF gene mutations associated with certain cancers, aiding in early diagnosis and de...

Starting from 760.32 SAR
Fatty Acid Disorders Profile

Fatty Acid Disorders Profile

Advanced analysis to measure blood fatty acid levels, aiding in early detection of metabolic disorders and ensuring effi...

Starting from 422.4 SAR