ATP7A Gene Menkes Disease Genetic Test sale cost 4400 AED
OCRL Gene Lowe Oculocerebrorenal Syndrome Genetic Test sale cost 4400 AED OCRL Gene Lowe Oculocerebrorenal Syndrome Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
LAMB2 Gene Nephrotic Syndrome Type 5 Genetic Test sale cost 4400 AED LAMB2 Gene Nephrotic Syndrome Type 5 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

ATP7A Gene Menkes Disease Genetic Test Cost

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

-21%

The ATP7A Gene Menkes Disease Genetic Test is a critical diagnostic tool used to identify mutations in the ATP7A gene, which are responsible for Menkes Disease. This condition, also known as Menkes kinky hair syndrome, is a genetic disorder that affects copper levels in the body, leading to severe developmental issues, neurological problems, and a characteristic appearance of brittle, kinky hair. Early detection through genetic testing is vital for the management and treatment of this disorder.

The test specifically looks for mutations in the ATP7A gene, which plays a key role in the regulation of copper transport and metabolism. A mutation in this gene disrupts the normal functioning of copper in the body, leading to the symptoms associated with Menkes Disease.

Offered by DNA Labs UAE, the ATP7A Gene Menkes Disease Genetic Test is conducted through a comprehensive analysis of the patient’s DNA, extracted from a blood sample. This advanced genetic testing helps in confirming the diagnosis, enabling early intervention strategies that can significantly improve the quality of life for affected individuals.

The cost of the ATP7A Gene Menkes Disease Genetic Test is 4400 AED. While the price may seem significant, the value of early and accurate diagnosis cannot be overstated, as it opens the door to potential treatments and specialized care that can mitigate the effects of the disease. DNA Labs UAE is known for its commitment to providing accurate, reliable, and timely genetic testing services, making it a trusted choice for this essential test.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

ATP7A Gene Menkes Disease Genetic Test

At DNA Labs UAE, we offer the ATP7A Gene Menkes disease genetic test. This test helps in diagnosing Menkes disease, a rare genetic disorder primarily affecting males. The test analyzes the ATP7A gene and identifies any mutations or variations that may be present.

Test Components and Price

The ATP7A Gene Menkes disease genetic test costs 4400.0 AED. The sample condition required for the test includes blood or extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

The report for the ATP7A Gene Menkes disease genetic test is delivered within 3 to 4 weeks. The test is conducted using Next-Generation Sequencing (NGS) technology.

Test Type and Doctor

The ATP7A Gene Menkes disease genetic test falls under the category of Hepatology, Nephrology, and Endocrinology disorders. It is recommended to consult with a General Physician for this test.

Test Department and Pre-Test Information

The ATP7A Gene Menkes disease genetic test is conducted in the Genetics department. Before undergoing the test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session is conducted to draw a pedigree chart of family members affected by ATP7A Gene Menkes disease.

Test Details

The ATP7A gene is responsible for producing a protein called copper-transporting ATPase 1 (ATP7A). This protein plays a crucial role in transporting copper within the body. Mutations in the ATP7A gene can lead to Menkes disease, a rare genetic disorder.

Menkes disease is characterized by a defect in copper absorption and transport, resulting in copper deficiency in various tissues and organs. This deficiency affects the development of the brain, bones, and other parts of the body.

The ATP7A Gene Menkes disease genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the ATP7A gene and identify any mutations or variations. NGS genetic testing allows for the simultaneous analysis of multiple genes, making it a powerful tool for diagnosing genetic disorders like Menkes disease.

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. In the case of Menkes disease, the ATP7A gene is analyzed to look for any mutations causing the disorder. Identifying the specific mutation in the ATP7A gene helps confirm a diagnosis of Menkes disease.

Furthermore, the information obtained from the ATP7A Gene Menkes disease genetic test can be used for genetic counseling and family planning purposes. It is crucial to note that genetic testing should be performed by healthcare professionals specializing in genetics and genetic disorders. They can provide appropriate counseling and guidance based on the test results.

Test Name ATP7A Gene Menkes disease Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ATP7A Gene Menkes disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ATP7A Gene Menkes disease NGS Genetic DNA Test gene ATP7A
Test Details

The ATP7A gene is responsible for producing a protein called copper-transporting ATPase 1 (ATP7A). This protein plays a crucial role in transporting copper within the body. Mutations in the ATP7A gene can lead to a rare genetic disorder known as Menkes disease.

Menkes disease is an X-linked recessive disorder that primarily affects males. It is characterized by a defect in copper absorption and transport, leading to copper deficiency in various tissues and organs. This deficiency affects the development of the brain, bones, and other parts of the body.

Next-generation sequencing (NGS) genetic testing can be used to analyze the ATP7A gene and identify any mutations or variations that may be present. This type of testing allows for the simultaneous analysis of multiple genes, making it a powerful tool for diagnosing genetic disorders like Menkes disease.

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. In the case of Menkes disease, the ATP7A gene would be analyzed to look for any mutations that may be causing the disorder.

By identifying the specific mutation in the ATP7A gene, NGS genetic testing can help confirm a diagnosis of Menkes disease. This information can also be used for genetic counseling and family planning purposes.

It is important to note that genetic testing should be performed by healthcare professionals who specialize in genetics and genetic disorders. They can provide appropriate counseling and guidance based on the test results.

SKU: TEST-3711 Category:

Related products