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SDHA Gene Mitochondrial Respiratory Chain Complex II Deficiency Genetic Test Cost

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

-21%

The SDHA gene plays a crucial role in the mitochondrial respiratory chain, specifically in Complex II, which is vital for energy production within cells. Deficiencies in Complex II can lead to a range of serious genetic disorders, including Leigh syndrome, cardiomyopathy, and mitochondrial encephalomyopathy. These conditions can manifest as neurological deficits, muscle weakness, heart problems, and metabolic disturbances.

The SDHA Gene Mitochondrial Respiratory Chain Complex II Deficiency Genetic Test is a specialized diagnostic tool used to identify mutations in the SDHA gene. By analyzing an individual’s DNA, this test can confirm or rule out the presence of genetic abnormalities affecting Complex II, assisting in the diagnosis, management, and treatment planning for affected patients.

This test is available at DNA Labs UAE, a leading facility in genetic diagnostics. The cost of the test is 4400 AED. DNA Labs UAE utilizes state-of-the-art technology and employs a team of genetic experts to ensure accurate and reliable results. This test is crucial for families with a history of mitochondrial or metabolic disorders, providing essential information for genetic counseling and decision-making regarding family planning.

Description

SDHA Gene Mitochondrial respiratory chain complex II deficiency Genetic Test

Test Name: SDHA Gene Mitochondrial respiratory chain complex II deficiency Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for SDHA Gene Mitochondrial respiratory chain complex II deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SDHA Gene Mitochondrial respiratory chain complex II deficiency.

Test Details: Mitochondrial respiratory chain complex II deficiency is a rare genetic disorder that affects the function of complex II (succinate dehydrogenase) in the mitochondrial respiratory chain. This complex is responsible for converting succinate into fumarate during cellular respiration. NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the rapid sequencing of large amounts of DNA. It can be used to identify mutations or variations in specific genes, including the SDHA gene. The SDHA gene provides instructions for making a protein called succinate dehydrogenase subunit A, which is a part of complex II. Mutations in this gene can disrupt the normal function of complex II, leading to mitochondrial respiratory chain complex II deficiency. NGS genetic testing for SDHA gene mutations can help diagnose mitochondrial respiratory chain complex II deficiency and determine the specific genetic cause of the condition. This information is important for understanding the underlying cause of the disease and for providing appropriate medical management and genetic counseling.

Test Name	SDHA Gene Mitochondrial respiratory chain 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 SDHA Gene Mitochondrial respiratory chain complex II deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SDHA Gene Mitochondrial respiratory chain complex II deficiency
Test Details	Mitochondrial respiratory chain complex II deficiency is a rare genetic disorder that affects the function of complex II (succinate dehydrogenase) in the mitochondrial respiratory chain. This complex is responsible for converting succinate into fumarate during cellular respiration. NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the rapid sequencing of large amounts of DNA. It can be used to identify mutations or variations in specific genes, including the SDHA gene. The SDHA gene provides instructions for making a protein called succinate dehydrogenase subunit A, which is a part of complex II. Mutations in this gene can disrupt the normal function of complex II, leading to mitochondrial respiratory chain complex II deficiency. NGS genetic testing for SDHA gene mutations can help diagnose mitochondrial respiratory chain complex II deficiency and determine the specific genetic cause of the condition. This information is important for understanding the underlying cause of the disease and for providing appropriate medical management and genetic counseling.