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POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B Genetic Test Cost

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

-21%

The POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the POLG gene. This gene is crucial for the maintenance of mitochondrial DNA, and mutations can lead to mitochondrial DNA depletion syndrome type 4B (MDDS4B), a rare genetic disorder. The syndrome is characterized by a spectrum of clinical features, including neurological and muscular impairments, which can vary significantly in severity among affected individuals.

This genetic test is instrumental in confirming the diagnosis of MDDS4B, enabling healthcare professionals to provide targeted treatment and management plans for patients. By analyzing the patient’s DNA, the test can identify specific mutations in the POLG gene that are responsible for the condition. Early diagnosis through genetic testing can be critical in managing symptoms and improving the quality of life for individuals with this syndrome.

The cost of the POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to detect the presence of mutations in the POLG gene accurately. Given the complexity and the specialized nature of this test, it represents a crucial step towards personalized medicine for patients suspected of having MDDS4B or related mitochondrial disorders.

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POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B Genetic Test

Test Details

POLG gene mitochondrial DNA depletion syndrome type 4B is a rare genetic disorder that affects the mitochondria, which are the energy-producing structures within cells. This condition is caused by mutations in the POLG gene, which is responsible for providing instructions for making an enzyme called DNA polymerase gamma.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of POLG gene mitochondrial DNA depletion syndrome type 4B, NGS genetic testing can identify specific mutations in the POLG gene that are associated with this condition.

Test Components and Price

  • Test Name: POLG Gene Mitochondrial DNA depletion syndrome type 4B Genetic Test
  • 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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for POLG Gene Mitochondrial DNA depletion syndrome type 4B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with POLG Gene Mitochondrial DNA depletion syndrome type 4B.

Test Details

POLG gene mitochondrial DNA depletion syndrome type 4B is a rare genetic disorder that affects the mitochondria, which are the energy-producing structures within cells. This condition is caused by mutations in the POLG gene, which is responsible for providing instructions for making an enzyme called DNA polymerase gamma.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of POLG gene mitochondrial DNA depletion syndrome type 4B, NGS genetic testing can identify specific mutations in the POLG gene that are associated with this condition.

The NGS genetic test for POLG gene mitochondrial DNA depletion syndrome type 4B involves obtaining a DNA sample, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the POLG gene.

This genetic test can help confirm a diagnosis of POLG gene mitochondrial DNA depletion syndrome type 4B in individuals who show symptoms of the condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known mutation.

The results of the NGS genetic test can provide valuable information for healthcare providers to guide treatment decisions and provide genetic counseling to affected individuals and their families. It is important to note that genetic testing may not be able to identify all possible mutations in the POLG gene, and a negative test result does not completely rule out the presence of the condition. Therefore, it is essential to consult with a healthcare professional to fully understand the implications of the test results.

Test Name POLG Gene Mitochondrial DNA depletion syndrome type 4B 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 POLG Gene Mitochondrial DNA depletion syndrome type 4B NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with POLG Gene Mitochondrial DNA depletion syndrome type 4B
Test Details

POLG gene mitochondrial DNA depletion syndrome type 4B is a rare genetic disorder that affects the mitochondria, which are the energy-producing structures within cells. This condition is caused by mutations in the POLG gene, which is responsible for providing instructions for making an enzyme called DNA polymerase gamma.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of POLG gene mitochondrial DNA depletion syndrome type 4B, NGS genetic testing can identify specific mutations in the POLG gene that are associated with this condition.

The NGS genetic test for POLG gene mitochondrial DNA depletion syndrome type 4B involves obtaining a DNA sample, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the POLG gene.

This genetic test can help confirm a diagnosis of POLG gene mitochondrial DNA depletion syndrome type 4B in individuals who show symptoms of the condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known mutation.

The results of the NGS genetic test can provide valuable information for healthcare providers to guide treatment decisions and provide genetic counseling to affected individuals and their families. It is important to note that genetic testing may not be able to identify all possible mutations in the POLG gene, and a negative test result does not completely rule out the presence of the condition. Therefore, it is essential to consult with a healthcare professional to fully understand the implications of the test results.

SKU: TEST-1724 Category:

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