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NGSMito Comprehensive NGS Genetic Test

4,400 د.إ

-27%

The NGSMito Comprehensive NGS Genetic Test, offered at DNA Labs UAE for a cost of 4400 AED, is a state-of-the-art genetic screening that utilizes Next Generation Sequencing (NGS) technology to provide a detailed analysis of the mitochondrial genome. This advanced test is designed to identify mutations and variations within the mitochondrial DNA (mtDNA) that could be indicative of various mitochondrial disorders, which are often complex and can affect multiple systems in the body. Mitochondrial diseases can lead to symptoms ranging from muscle weakness and neurological issues to more severe conditions affecting organ function. The comprehensive nature of this test makes it a powerful tool for individuals seeking insights into their genetic makeup concerning mitochondrial health, potentially guiding diagnosis, treatment, and management of mitochondrial-related conditions. DNA Labs UAE ensures accuracy and reliability in their testing processes, making the NGSMito Comprehensive NGS Genetic Test a valuable resource for those looking to understand their genetic predisposition to mitochondrial diseases.

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  • This test is not intended for medical diagnosis or treatment
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NGSMito Comprehensive NGS Genetic Test

Cost: AED 4400.0

Test Name

NGSMito Comprehensive NGS Genetic DNA Test

Components

Price: AED 4400.0

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 NGSMito Comprehensive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NGSMito Comprehensive.

Test Details

The NGSMito Comprehensive NGS Genetic DNA Test is a genetic test that analyzes an individual’s mitochondrial DNA (mtDNA) using next-generation sequencing (NGS) technology. Mitochondria are the energy-producing organelles within cells, and mtDNA is the DNA found within mitochondria.

The NGSMito Comprehensive test analyzes the entire mtDNA genome, which includes over 16,000 base pairs. This test can identify genetic variants, mutations, and deletions within the mtDNA that may be associated with various medical conditions, including mitochondrial diseases, neurodegenerative disorders, and metabolic disorders.

The NGSMito Comprehensive test is typically ordered by healthcare providers for individuals who have symptoms or a family history of mitochondrial disorders. The test requires a blood or saliva sample, which is then sent to a specialized laboratory for analysis. Results are typically available within several weeks.

Overall, the NGSMito Comprehensive NGS Genetic DNA Test is a powerful tool for identifying potential genetic causes of mitochondrial disorders and other medical conditions associated with mtDNA mutations. It can help healthcare providers make more informed decisions about patient care and treatment options.

 

Test NameNGSMito Comprehensive NGS Genetic DNA Test
Components 
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeNeurological Disorders
DoctorNeurologist
Test Department:Genetics
Pre Test InformationClinical History of Patient who is going for NGSMito Comprehensive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NGSMito Comprehensive
Test Details

The NGSMito Comprehensive NGS Genetic DNA Test is a genetic test that analyzes an individual’s mitochondrial DNA (mtDNA) using next-generation sequencing (NGS) technology. Mitochondria are the energy-producing organelles within cells, and mtDNA is the DNA found within mitochondria.

The NGSMito Comprehensive test analyzes the entire mtDNA genome, which includes over 16,000 base pairs. This test can identify genetic variants, mutations, and deletions within the mtDNA that may be associated with various medical conditions, including mitochondrial diseases, neurodegenerative disorders, and metabolic disorders.

The NGSMito Comprehensive test is typically ordered by healthcare providers for individuals who have symptoms or a family history of mitochondrial disorders. The test requires a blood or saliva sample, which is then sent to a specialized laboratory for analysis. Results are typically available within several weeks.

Overall, the NGSMito Comprehensive NGS Genetic DNA Test is a powerful tool for identifying potential genetic causes of mitochondrial disorders and other medical conditions associated with mtDNA mutations. It can help healthcare providers make more informed decisions about patient care and treatment options.