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SDHD Gene Mitochondrial Complex II Deficiency Genetic Test

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

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The SDHD Gene Mitochondrial Complex II Deficiency Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the SDHD gene that can lead to mitochondrial complex II deficiency. This condition is part of a group of disorders that affect the mitochondrial respiratory chain, crucial for energy production in cells. Mutations in the SDHD gene can disrupt this process, leading to a variety of symptoms, including muscle weakness, neurodegenerative issues, and in severe cases, organ failure.

The test is crucial for individuals showing symptoms suggestive of mitochondrial disorders or for those with a family history of such conditions. Early detection through this genetic test can aid in the management and treatment planning for affected individuals, potentially improving quality of life and outcomes.

DNA Labs UAE offers this test at a cost of 4400 AED. The testing process involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory for the presence of mutations in the SDHD gene. The results from this test can provide valuable information for patients and healthcare providers, guiding decisions on treatment and management of the condition.

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SDHD Gene Mitochondrial complex II deficiency Genetic Test

At DNA Labs UAE, we offer the SDHD Gene Mitochondrial complex II deficiency Genetic Test at a cost of 4400.0 AED. This test analyzes the SDHD gene for mutations or variants associated with mitochondrial complex II deficiency using next-generation sequencing (NGS) technology.

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

Before undergoing the SDHD Gene Mitochondrial complex II deficiency NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by SDHD Gene Mitochondrial complex II deficiency.

Test Details

The SDHD gene mitochondrial complex II deficiency NGS genetic test is used to identify mutations or variants associated with mitochondrial complex II deficiency. Mitochondrial complex II, also known as succinate dehydrogenase, plays a crucial role in the electron transport chain and energy generation. Mutations in the SDHD gene can lead to a malfunction of complex II, resulting in various symptoms and health problems.

The NGS genetic test involves sequencing the entire coding region of the SDHD gene to identify any mutations or variants. This test can help diagnose individuals with mitochondrial complex II deficiency and guide treatment decisions. NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup. It is a highly sensitive and efficient method for identifying genetic variations, including single nucleotide variants, insertions, deletions, and structural variants, in the SDHD gene.

The results of the SDHD gene mitochondrial complex II deficiency NGS genetic test can assist healthcare providers in determining appropriate management and treatment options. It also provides valuable information for genetic counseling and family planning purposes.

Test Name SDHD Gene Mitochondrial complex II deficiency 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 SDHD Gene Mitochondrial complex II deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SDHD Gene Mitochondrial complex II deficiency
Test Details

SDHD gene mitochondrial complex II deficiency NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the SDHD gene for mutations or variants associated with mitochondrial complex II deficiency.

Mitochondrial complex II deficiency is a rare genetic disorder that affects the function of complex II, also known as succinate dehydrogenase, in the mitochondria. This complex plays a crucial role in the electron transport chain, which is responsible for generating energy in the form of ATP. Mutations in the SDHD gene can lead to a malfunction of complex II, resulting in a range of symptoms and health problems.

The NGS genetic test for SDHD gene mitochondrial complex II deficiency involves sequencing the entire coding region of the SDHD gene to identify any mutations or variants that may be present. This test can help diagnose individuals with mitochondrial complex II deficiency and guide treatment decisions.

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup. It is a highly sensitive and efficient method for identifying genetic variations, including single nucleotide variants, insertions, deletions, and structural variants, in the SDHD gene.

The results of the SDHD gene mitochondrial complex II deficiency NGS genetic test can help healthcare providers determine the appropriate management and treatment options for affected individuals. It can also provide valuable information for genetic counseling and family planning purposes.

SKU: TEST-1699 Category:

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