RRM2B Gene Mitochondrial DNA Depletion Syndrome 8B MNGIE Type Genetic Test sale cost 4400 AED
NDUFS1 Gene Mitochondrial Complex I Deficiency Genetic Test sale cost 4400 AED NDUFS1 Gene Mitochondrial Complex I Deficiency Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
POMK Gene Muscle-Eye-Brain Disease POMK Related Genetic Test sale cost 4400 AED POMK Gene Muscle-Eye-Brain Disease POMK Related 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!

RRM2B Gene Mitochondrial DNA Depletion Syndrome 8B MNGIE Type Genetic Test Cost

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

-21%

The RRM2B Gene Mitochondrial DNA Depletion Syndrome 8B (MNGIE Type) genetic test is a specialized diagnostic examination offered by DNA Labs UAE, aimed at detecting mutations in the RRM2B gene. These mutations are responsible for a rare condition known as Mitochondrial DNA Depletion Syndrome 8B, also referred to as the MNGIE type. This syndrome is characterized by a range of symptoms including gastrointestinal dysfunctions, peripheral neuropathy, and progressive external ophthalmoplegia, stemming from a reduction in mitochondrial DNA within cells.

The test is crucial for the accurate diagnosis and understanding of the syndrome, enabling healthcare providers to tailor treatment and management strategies effectively for affected individuals. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the test involves collecting a DNA sample from the patient, usually through a blood draw, and then analyzing it for specific mutations in the RRM2B gene.

The cost of the RRM2B Gene Mitochondrial DNA Depletion Syndrome 8B MNGIE Type genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to identify the genetic markers of the syndrome, providing essential information for patients and their families. By confirming the diagnosis, individuals can gain access to supportive therapies and interventions that may improve quality of life and manage symptoms associated with the condition.

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

RRM2B Gene Mitochondrial DNA depletion syndrome 8B MNGIE type Genetic Test

Test Name: RRM2B Gene Mitochondrial DNA depletion syndrome 8B MNGIE type Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 RRM2B Gene Mitochondrial DNA depletion syndrome 8B, MNGIE type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RRM2B Gene Mitochondrial DNA depletion syndrome 8B, MNGIE type.

Test Details

The RRM2B gene is associated with a condition called Mitochondrial DNA depletion syndrome 8B, MNGIE type. This syndrome is characterized by a progressive loss of mitochondrial DNA, leading to a variety of symptoms including muscle weakness, gastrointestinal issues, and neurological problems.

NGS Genetic Test refers to Next-Generation Sequencing Genetic Test, which is a high-throughput sequencing technology used to analyze multiple genes simultaneously. In the context of RRM2B gene and Mitochondrial DNA depletion syndrome 8B, MNGIE type, an NGS Genetic Test can be used to detect any mutations or variations in the RRM2B gene that may be causing the syndrome.

The test involves extracting DNA from a patient’s blood or tissue sample and sequencing the RRM2B gene using NGS technology. The obtained sequence data is then compared to a reference sequence to identify any genetic changes or mutations. By identifying specific mutations in the RRM2B gene, the NGS Genetic Test can help in confirming a diagnosis of Mitochondrial DNA depletion syndrome 8B, MNGIE type.

It can also be useful for genetic counseling and providing information about the risk of passing the condition to future generations. Additionally, NGS Genetic Testing can aid in the development of personalized treatment plans and monitoring the progression of the disease.

Test Name RRM2B Gene Mitochondrial DNA depletion syndrome 8B MNGIE type 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 RRM2B Gene Mitochondrial DNA depletion syndrome 8B, MNGIE type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RRM2B Gene Mitochondrial DNA depletion syndrome 8B, MNGIE type
Test Details

The RRM2B gene is associated with a condition called Mitochondrial DNA depletion syndrome 8B, MNGIE type. This syndrome is characterized by a progressive loss of mitochondrial DNA, leading to a variety of symptoms including muscle weakness, gastrointestinal issues, and neurological problems.

NGS Genetic Test refers to Next-Generation Sequencing Genetic Test, which is a high-throughput sequencing technology used to analyze multiple genes simultaneously. In the context of RRM2B gene and Mitochondrial DNA depletion syndrome 8B, MNGIE type, an NGS Genetic Test can be used to detect any mutations or variations in the RRM2B gene that may be causing the syndrome.

The test involves extracting DNA from a patient’s blood or tissue sample and sequencing the RRM2B gene using NGS technology. The obtained sequence data is then compared to a reference sequence to identify any genetic changes or mutations.

By identifying specific mutations in the RRM2B gene, the NGS Genetic Test can help in confirming a diagnosis of Mitochondrial DNA depletion syndrome 8B, MNGIE type. It can also be useful for genetic counseling and providing information about the risk of passing the condition to future generations. Additionally, NGS Genetic Testing can aid in the development of personalized treatment plans and monitoring the progression of the disease.

SKU: TEST-1720 Category:

Related products