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PAK3 Gene Mental Retardation X-Linked Type 30 Genetic Test Cost

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

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The “PAK3 Gene Mental Retardation X-Linked Type 30 Genetic Test” is a specialized diagnostic procedure aimed at identifying mutations in the PAK3 gene, which are associated with mental retardation X-linked type 30 (MRX30). This condition, primarily affecting males due to its X-linked inheritance pattern, is characterized by various degrees of intellectual disability and, in some cases, additional neurological or physical symptoms. The PAK3 gene plays a crucial role in brain development and function, and mutations in this gene can disrupt these processes, leading to the symptoms observed in affected individuals.

This genetic test involves analyzing the patient’s DNA to detect mutations in the PAK3 gene that are known to cause MRX30. It is a critical tool for accurate diagnosis, allowing for better understanding and management of the condition. It also provides essential information for family planning and genetic counseling for families affected by MRX30.

The test is available at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the PAK3 gene. For families and individuals seeking answers about intellectual disability and potential genetic causes, this test represents a valuable resource for diagnosis and guidance on managing X-linked mental retardation type 30.

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PAK3 Gene Mental Retardation X-linked Type 30 Genetic Test

Are you concerned about the possibility of mental retardation in your family? DNA Labs UAE offers the PAK3 Gene Mental Retardation X-linked Type 30 Genetic Test, which can provide valuable insights into this condition. In this blog, we will discuss the symptoms, diagnosis, and cost of this genetic test.

Test Details

The PAK3 gene is located on the X chromosome and is associated with X-linked intellectual disability. Mutations in this gene can lead to a condition called mental retardation, X-linked type 30 (MRX30). To analyze the DNA sequence of an individual’s genes, we use NGS (Next-Generation Sequencing) technology. This method allows us to identify genetic variations or mutations that may be causing MRX30.

Symptoms and Diagnosis

The symptoms of MRX30 can vary widely, but common signs include intellectual disability, delayed speech and language development, behavioral problems, and seizures. If you suspect that your child or family member may have MRX30, it is important to consult with a neurologist who specializes in neurological disorders. A thorough clinical history of the patient is necessary before proceeding with the genetic test.

Test Components and Price

The PAK3 Gene Mental Retardation X-linked Type 30 Genetic Test costs AED 4400.0. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. The report delivery time is approximately 3 to 4 weeks.

Genetic Counseling and Family Planning

If MRX30 is confirmed through genetic testing, it is crucial to seek genetic counseling. Our genetic counselors can help draw a pedigree chart of family members affected by MRX30, providing important information for family planning and understanding the inheritance pattern of this condition.

Importance of NGS Genetic Testing

NGS genetic testing is a powerful tool in the field of genetics. It allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup. This technology has revolutionized our ability to identify and understand genetic disorders.

Qualified Healthcare Professionals

It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics. Our team of neurologists and geneticists are experts in the field and can guide you through the testing process. They will also help you understand the implications of the test results and provide the necessary support.

Don’t let the fear of the unknown hold you back. Contact DNA Labs UAE today to schedule the PAK3 Gene Mental Retardation X-linked Type 30 Genetic Test and gain valuable insights into your genetic health.

Test Name PAK3 Gene Mental retardation X-linked type 30 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 PAK3 Gene Mental retardation, X-linked type 30 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PAK3 Gene Mental retardation, X-linked type 30
Test Details

The PAK3 gene is located on the X chromosome and is associated with X-linked intellectual disability. Mutations in this gene can lead to a condition called mental retardation, X-linked type 30 (MRX30).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the identification of genetic variations or mutations that may be causing a particular condition or disease.

In the case of MRX30, NGS genetic testing can be used to sequence the PAK3 gene and identify any mutations or variations that may be present. This can help in confirming a diagnosis of MRX30 and can also provide important information for genetic counseling and family planning.

NGS genetic testing is a powerful tool in the field of genetics and has revolutionized our ability to identify and understand genetic disorders. It allows for the analysis of multiple genes simultaneously and provides a comprehensive view of an individual’s genetic makeup.

It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics. They can provide guidance and support throughout the testing process and help individuals and families understand the implications of the results.

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