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UQCRC2 Gene Mitochondrial Complex III Deficiency Genetic Test Cost

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

-21%

The UQCRC2 Gene Mitochondrial Complex III Deficiency Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the UQCRC2 gene. These mutations can lead to mitochondrial complex III deficiency, a rare genetic disorder that affects the body’s ability to generate energy at the cellular level. Mitochondrial complex III is a critical component of the mitochondrial respiratory chain, and its deficiency can lead to a wide range of clinical manifestations, including muscle weakness, heart problems, growth retardation, and neurological issues, among others.

The test is crucial for individuals who exhibit symptoms suggestive of mitochondrial disorders or have a family history of such conditions. Early and accurate diagnosis through this genetic test enables healthcare providers to tailor treatment plans more effectively, potentially improving the quality of life for affected individuals.

Performed at the state-of-the-art facilities of DNA Labs UAE, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific mutations in the UQCRC2 gene. The cost of the test is set at 4400 AED, reflecting the intricate technologies and expert analysis involved in identifying the genetic mutations responsible for the condition.

Given the complexity of mitochondrial diseases and the importance of precise genetic information for management and treatment, the UQCRC2 Gene Mitochondrial Complex III Deficiency Genetic Test represents a valuable resource for patients and their families seeking answers and support in managing these challenging conditions.

Description

UQCRC2 Gene Mitochondrial complex III deficiency Genetic Test

Test Name: UQCRC2 Gene Mitochondrial complex III deficiency 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 UQCRC2 Gene Mitochondrial complex III deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UQCRC2 Gene Mitochondrial complex III deficiency.

Test Details:

The UQCRC2 gene is one of the genes associated with mitochondrial complex III deficiency, which is a genetic disorder affecting the function of Complex III in the mitochondrial electron transport chain. This deficiency can lead to a wide range of symptoms including muscle weakness, exercise intolerance, developmental delays, and neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly and simultaneously analyze multiple genes. In the context of mitochondrial complex III deficiency, NGS genetic testing can be used to identify mutations or variants in the UQCRC2 gene, as well as other genes associated with this disorder.

NGS genetic testing is a powerful tool that allows for the detection of a large number of genetic variants in a short amount of time. It can provide valuable information for diagnosis, prognosis, and treatment options for individuals with mitochondrial complex III deficiency. However, it is important to note that NGS genetic testing may not identify all possible genetic variants, and additional testing or clinical evaluation may be necessary for a complete diagnosis.

Test Name	UQCRC2 Gene Mitochondrial complex III 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 UQCRC2 Gene Mitochondrial complex III deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with UQCRC2 Gene Mitochondrial complex III deficiency
Test Details	The UQCRC2 gene is one of the genes associated with mitochondrial complex III deficiency, which is a genetic disorder affecting the function of Complex III in the mitochondrial electron transport chain. This deficiency can lead to a wide range of symptoms including muscle weakness, exercise intolerance, developmental delays, and neurological problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly and simultaneously analyze multiple genes. In the context of mitochondrial complex III deficiency, NGS genetic testing can be used to identify mutations or variants in the UQCRC2 gene, as well as other genes associated with this disorder. NGS genetic testing is a powerful tool that allows for the detection of a large number of genetic variants in a short amount of time. It can provide valuable information for diagnosis, prognosis, and treatment options for individuals with mitochondrial complex III deficiency. However, it is important to note that NGS genetic testing may not identify all possible genetic variants, and additional testing or clinical evaluation may be necessary for a complete diagnosis.