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UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 Genetic Test Cost

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

-21%

The UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 Genetic Test is a specialized diagnostic examination conducted at DNA Labs UAE, designed to detect mutations in the UQCC2 gene. These mutations are associated with Mitochondrial Complex III Deficiency, Nuclear Type 7, a rare genetic disorder that affects the body’s ability to generate energy. The test is crucial for identifying individuals who may be affected by this condition, which can lead to various symptoms ranging from muscle weakness, heart problems, to growth delays, depending on the severity of the deficiency.

Given the complexity and the specific expertise required to perform and interpret this test, it is priced at 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals skilled in genetic diagnostics, ensuring high accuracy and reliability of the test results. This genetic test is an essential tool for healthcare providers in diagnosing the condition early and accurately, allowing for appropriate management strategies to be implemented, enhancing the quality of life for affected individuals.

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UQCC2 Gene Mitochondrial complex III deficiency nuclear type 7 Genetic Test

Components: UQCC2 Gene Mitochondrial complex III deficiency nuclear type 7 Genetic Test

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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for UQCC2 Gene Mitochondrial complex III deficiency, nuclear type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Mitochondrial complex III deficiency, nuclear type 7.

Test Details

The UQCC2 gene is associated with mitochondrial complex III deficiency, nuclear type 7. Mitochondrial complex III deficiency is a rare genetic disorder that affects the function of complex III in the mitochondrial electron transport chain. This deficiency can lead to a variety of symptoms, including muscle weakness, exercise intolerance, developmental delay, and neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic mutations or variants associated with a particular condition, such as UQCC2 gene mutations in mitochondrial complex III deficiency.

The NGS genetic test for UQCC2 gene mutations can help in diagnosing individuals suspected of having mitochondrial complex III deficiency, nuclear type 7. It involves obtaining a DNA sample, usually through a blood or saliva sample, and analyzing the genetic sequence of the UQCC2 gene using NGS technology. The test can identify specific mutations or variants in the UQCC2 gene that may be causing the mitochondrial complex III deficiency.

The results of the NGS genetic test can provide valuable information for genetic counseling, as well as guide treatment options and management strategies for individuals affected by mitochondrial complex III deficiency, nuclear type 7. It is important to consult with a healthcare professional or genetic counselor to understand the implications of the test results and discuss appropriate next steps.

Test Name UQCC2 Gene Mitochondrial complex III deficiency nuclear type 7 Genetic 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for UQCC2 Gene Mitochondrial complex III deficiency, nuclear type 7 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mitochondrial complex III deficiency, nuclear type 7
Test Details

The UQCC2 gene is associated with mitochondrial complex III deficiency, nuclear type 7. Mitochondrial complex III deficiency is a rare genetic disorder that affects the function of complex III in the mitochondrial electron transport chain. This deficiency can lead to a variety of symptoms, including muscle weakness, exercise intolerance, developmental delay, and neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic mutations or variants associated with a particular condition, such as UQCC2 gene mutations in mitochondrial complex III deficiency.

The NGS genetic test for UQCC2 gene mutations can help in diagnosing individuals suspected of having mitochondrial complex III deficiency, nuclear type 7. It involves obtaining a DNA sample, usually through a blood or saliva sample, and analyzing the genetic sequence of the UQCC2 gene using NGS technology. The test can identify specific mutations or variants in the UQCC2 gene that may be causing the mitochondrial complex III deficiency.

The results of the NGS genetic test can provide valuable information for genetic counseling, as well as guide treatment options and management strategies for individuals affected by mitochondrial complex III deficiency, nuclear type 7. It is important to consult with a healthcare professional or genetic counselor to understand the implications of the test results and discuss appropriate next steps.

SKU: TEST-2550