MGME1 Gene Mitochondrial DNA Depletion Syndrome Type 11 Genetic Test
At DNA Labs UAE, we offer the MGME1 Gene Mitochondrial DNA depletion syndrome type 11 Genetic Test. This test helps in diagnosing and understanding this genetic condition.
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
Neurological Disorders
Doctor
Neurologist
Test Department
Genetics
Pre Test Information
Clinical History of Patient who is going for MGME1 Gene Mitochondrial DNA depletion syndrome type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MGME1 Gene Mitochondrial DNA depletion syndrome type 11.
Test Details
The MGME1 gene is associated with a condition called mitochondrial DNA depletion syndrome type 11. This syndrome is characterized by a decrease in the amount of mitochondrial DNA (mtDNA) in cells, leading to impaired mitochondrial function.
NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technologies to rapidly sequence large amounts of DNA. In the case of MGME1 gene testing, NGS can be used to analyze the DNA sequence of the gene and identify any mutations or variants that may be present. This can help diagnose mitochondrial DNA depletion syndrome type 11 and provide information about the specific genetic changes causing the condition.
Genetic testing for MGME1 gene mutations can be useful for individuals with symptoms suggestive of mitochondrial DNA depletion syndrome type 11, as well as for their family members who may be at risk of carrying the same genetic mutation. It can help in confirming the diagnosis, providing information about the prognosis, and guiding treatment options for affected individuals.
Test Name | MGME1 Gene Mitochondrial DNA depletion syndrome type 11 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 MGME1 Gene Mitochondrial DNA depletion syndrome type 11 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MGME1 Gene Mitochondrial DNA depletion syndrome type 11 |
Test Details |
The MGME1 gene is associated with a condition called mitochondrial DNA depletion syndrome type 11. This syndrome is characterized by a decrease in the amount of mitochondrial DNA (mtDNA) in cells, leading to impaired mitochondrial function. NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technologies to rapidly sequence large amounts of DNA. In the case of MGME1 gene testing, NGS can be used to analyze the DNA sequence of the gene and identify any mutations or variants that may be present. This can help diagnose mitochondrial DNA depletion syndrome type 11 and provide information about the specific genetic changes causing the condition. Genetic testing for MGME1 gene mutations can be useful for individuals with symptoms suggestive of mitochondrial DNA depletion syndrome type 11, as well as for their family members who may be at risk of carrying the same genetic mutation. It can help in confirming the diagnosis, providing information about the prognosis, and guiding treatment options for affected individuals. |