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MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test Cost

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

-21%

MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 (MTDPS6) is a rare genetic disorder characterized by a significant reduction in mitochondrial DNA (mtDNA) in affected tissues, leading to a spectrum of clinical manifestations including liver dysfunction, neurological deficits, and muscle weakness. This condition is caused by mutations in the MPV17 gene, which plays a crucial role in the maintenance of mitochondrial DNA.

To diagnose this condition, a genetic test targeting the MPV17 gene can be conducted. This test is crucial for confirming the diagnosis, understanding the disease’s progression, and for family planning purposes. DNA Labs UAE offers this specialized genetic testing service. The test involves analyzing the patient’s DNA to identify mutations in the MPV17 gene that are responsible for Mitochondrial DNA Depletion Syndrome Type 6.

The cost of the MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is conducted in a state-of-the-art laboratory setting by skilled geneticists and laboratory technicians. The process includes collecting a DNA sample, usually through a blood draw or cheek swab, followed by detailed analysis using advanced genetic sequencing technologies.

Upon completion of the test, a detailed report is provided to the patient or the ordering physician, outlining the findings and offering insights into the genetic makeup of the individual concerning the MPV17 gene. This information is vital for devising a personalized management plan for affected individuals and offers the possibility of genetic counseling for families.

Description

MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test

At DNA Labs UAE, we offer the MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test. This test helps in the diagnosis of a rare genetic disorder known as mitochondrial DNA depletion syndrome type 6 (MTDPS6). MTDPS6 affects the mitochondria, which are responsible for producing energy in the cells.

Test Details

The MPV17 gene is associated with MTDPS6. This genetic disorder is characterized by a decrease in the amount of mitochondrial DNA (mtDNA) in affected tissues, leading to various symptoms. Our Next-Generation Sequencing (NGS) technology allows us to analyze multiple genes simultaneously. In the case of MTDPS6, NGS is used to sequence the MPV17 gene and identify any mutations or variations that may be present.

Test Components and Price

The MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.

Report Delivery

After the sample is collected, the report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test falls under the category of Neurological Disorders. It is recommended to consult a Neurologist for this test.

Test Department and Pre Test Information

This test is conducted in our Genetics department. Before the test, it is important to provide the clinical history of the patient who is going for the MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with MTDPS6.

How the Test Works

NGS genetic testing for MTDPS6 involves collecting a sample of DNA, usually through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology, which can analyze the entire coding region of the MPV17 gene. The results of the test can help confirm a diagnosis of MTDPS6 and provide information about the inheritance pattern of the condition.

Referral and Genetic Counseling

It’s important to note that genetic testing for MTDPS6 is typically done in specialized laboratories and may require a referral from a healthcare provider who suspects the condition based on the individual’s symptoms and medical history. Genetic counseling is also recommended both before and after genetic testing to help individuals and families understand the implications of the test results and make informed decisions about their healthcare.

Test Name	MPV17 Gene Mitochondrial DNA depletion syndrome type 6 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 MPV17 Gene Mitochondrial DNA depletion syndrome type 6 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MPV17 Gene Mitochondrial DNA depletion syndrome type 6
Test Details	The MPV17 gene is associated with mitochondrial DNA depletion syndrome type 6 (MTDPS6). This is a rare genetic disorder that affects the mitochondria, which are responsible for producing energy in the cells. MTDPS6 is characterized by a decrease in the amount of mitochondrial DNA (mtDNA) in affected tissues, leading to a variety of symptoms. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of MTDPS6, NGS can be used to sequence the MPV17 gene and identify any mutations or variations that may be present. This can help in the diagnosis of MTDPS6 and provide information about the specific genetic cause of the disorder. NGS genetic testing for MTDPS6 typically involves collecting a sample of DNA, usually through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology, which can analyze the entire coding region of the MPV17 gene. The results of the test can help confirm a diagnosis of MTDPS6 and provide information about the inheritance pattern of the condition. It’s important to note that genetic testing for MTDPS6 is typically done in specialized laboratories and may require a referral from a healthcare provider who suspects the condition based on the individual’s symptoms and medical history. Genetic counseling is also recommended both before and after genetic testing to help individuals and families understand the implications of the test results and make informed decisions about their healthcare.

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