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TSPAN7 Gene Mental Retardation X-Linked Type 58 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The TSPAN7 gene, associated with X-linked mental retardation type 58, plays a crucial role in cognitive development and function. Mutations in this gene can lead to a spectrum of intellectual disabilities, often accompanied by other neurological symptoms. Recognizing the importance of early and accurate diagnosis, DNA Labs UAE offers a specialized genetic test aimed at detecting mutations in the TSPAN7 gene. Priced at 4400 AED, this test is a valuable tool for families seeking answers to developmental delays and intellectual challenges in their loved ones. By identifying specific genetic alterations, the test not only facilitates a precise diagnosis but also aids in tailoring appropriate interventions and support, ultimately improving the quality of life for affected individuals.

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TSPAN7 Gene Mental Retardation X-Linked Type 58 Genetic Test

Welcome to DNA Labs UAE, where we offer the TSPAN7 Gene Mental Retardation X-Linked Type 58 Genetic Test. This test is designed to help diagnose a genetic condition known as Mental Retardation, X-Linked Type 58 (MRX58). MRX58 is characterized by intellectual disability, delayed development, and other neurological abnormalities.

Test Details

The TSPAN7 gene is associated with MRX58, which is inherited in an X-linked pattern. This means that the gene mutation is located on the X chromosome. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously, helping us identify genetic mutations or variations that may be responsible for MRX58.

Test Components and Price

The TSPAN7 Gene Mental Retardation X-Linked Type 58 Genetic Test costs 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA Card. The report delivery typically takes 3 to 4 weeks.

Diagnosis Process

If you suspect that you or someone you know may have MRX58, we recommend consulting with a neurologist. They will gather the clinical history of the patient and conduct a genetic counseling session to draw a pedigree chart of affected family members. This information will help in the diagnosis process.

Test Method

Our Genetics department utilizes NGS technology to analyze the DNA of individuals suspected to have MRX58. This involves identifying any mutations in the TSPAN7 gene, which is associated with the condition.

Benefits of the Test

The results of the TSPAN7 Gene Mental Retardation X-Linked Type 58 Genetic Test provide valuable information for genetic counseling, treatment planning, and understanding the inheritance pattern of MRX58 within a family. It can help healthcare providers make informed decisions regarding patient care.

Contact a Neurologist

If you believe that you or someone you know may benefit from the TSPAN7 Gene Mental Retardation X-Linked Type 58 Genetic Test, we recommend consulting with a neurologist. They can provide further guidance and determine if this test is appropriate for your situation.

Test Name TSPAN7 Gene Mental retardation X-linked type 58 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TSPAN7 Gene Mental retardation, X-linked type 58 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TSPAN7 Gene Mental retardation, X-linked type 58
Test Details

The TSPAN7 gene is associated with a genetic condition called Mental Retardation, X-Linked Type 58 (MRX58). This condition is characterized by intellectual disability, delayed development, and other neurological abnormalities. MRX58 is inherited in an X-linked pattern, meaning that the gene mutation is located on the X chromosome.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of genetic mutations or variations that may be responsible for a particular condition. In the case of MRX58, NGS genetic testing can be used to detect mutations in the TSPAN7 gene, which can help in diagnosing the condition.

If an individual is suspected to have MRX58, a healthcare provider may recommend NGS genetic testing to confirm the diagnosis. This test involves analyzing the DNA of the individual to identify any mutations in the TSPAN7 gene. The results of the test can provide valuable information for genetic counseling, treatment planning, and understanding the inheritance pattern of the condition within a family.