Fragile X Syndrome (FXS) is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. It is the most common form of inherited intellectual disability in males and a significant cause of intellectual disability in females. The condition is caused by a mutation in the FMR1 gene on the X chromosome. Detecting this mutation is crucial for diagnosis, management, and understanding the inheritance pattern within families. DNA Labs UAE offers a comprehensive testing service for Fragile X Syndrome through the FMR1 Detection by PCR Test, priced at 1500 AED. This test is a vital resource for families seeking answers about this condition.
Symptoms of Fragile X Syndrome
Fragile X Syndrome presents a wide array of symptoms, which can vary significantly in severity among affected individuals. Some common symptoms include:
- Intellectual disability or learning challenges
- Behavioral and emotional difficulties
- Physical features such as a long face, large ears, and flexible joints
- Speech and language delays
- Sensitivity to sensory stimuli
- Seizures in some individuals
It is important to note that females with Fragile X Syndrome may have milder symptoms than males. Early detection and intervention can significantly improve the quality of life for those affected by FXS.
FMR1 Detection by PCR Test
The FMR1 Detection by PCR Test is a sophisticated diagnostic tool used to identify mutations in the FMR1 gene, which causes Fragile X Syndrome. This test employs Polymerase Chain Reaction (PCR) technology to amplify the DNA segment of interest, making it easier to analyze for mutations. It is a highly sensitive and specific test that can detect both full mutations and premutations in the FMR1 gene.
The test is recommended for individuals with intellectual disabilities, autism spectrum disorders, or a family history of Fragile X Syndrome. It is also advised for women with a family history of premature ovarian failure or unexplained infertility, as these conditions can be related to FMR1 gene mutations.
Understanding the Test Process
The process for undergoing the FMR1 Detection by PCR Test at DNA Labs UAE is straightforward. A sample of the individual’s blood is collected and sent to the laboratory for analysis. The test focuses on identifying the CGG repeat expansion in the FMR1 gene, which is indicative of Fragile X Syndrome. Results are typically available within a few weeks and are thoroughly explained by a genetic counselor or medical professional.
Why Choose DNA Labs UAE for FMR1 Detection?
Choosing DNA Labs UAE for FMR1 Detection by PCR Test ensures access to state-of-the-art testing facilities and highly qualified professionals. With a cost of 1500 AED, the test is both accessible and affordable, providing families with crucial information for managing Fragile X Syndrome. Additionally, DNA Labs UAE offers comprehensive support throughout the testing process, including pre-test counseling and post-test interpretation of results.
For more information about the Fragile X Syndrome FMR1 Detection by PCR Test and to schedule your appointment, please visit DNA Labs UAE.
Fragile X Syndrome is a challenging condition, but early detection and intervention can make a significant difference. The FMR1 Detection by PCR Test offered by DNA Labs UAE is a crucial tool in the diagnosis and management of this condition, providing families with the knowledge and support they need to navigate the complexities of Fragile X Syndrome.
