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NDUFAF1 Gene Mitochondrial Complex I Deficiency Genetic Test Cost

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

-21%

The NDUFAF1 Gene Mitochondrial Complex I Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the NDUFAF1 gene. These mutations are linked to mitochondrial complex I deficiency, a condition that affects mitochondrial function, leading to a range of symptoms including muscle weakness, heart problems, and neurological issues. The test, priced at 4400 AED, involves analyzing the patient’s DNA to detect any abnormalities in the NDUFAF1 gene, which plays a crucial role in the assembly and function of mitochondrial complex I. By identifying these mutations, healthcare providers can better understand the condition, leading to more targeted treatments and management strategies for affected individuals.

Description

NDUFAF1 Gene Mitochondrial complex I deficiency Genetic Test

Components: NDUFAF1 Gene Mitochondrial complex I deficiency 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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for NDUFAF1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF1 Gene Mitochondrial complex I deficiency.

Test Details:

The NDUFAF1 gene is responsible for encoding a protein that is involved in the assembly and stability of mitochondrial complex I, which is a crucial component of the mitochondrial respiratory chain. Mitochondrial complex I deficiency refers to a condition where there is a malfunction or deficiency in the function of this complex.

NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the NDUFAF1 gene that may be responsible for the deficiency. By sequencing the DNA of an individual, NGS can identify specific genetic changes that may be affecting the function of the NDUFAF1 gene.

This information can help diagnose mitochondrial complex I deficiency and guide treatment decisions. NGS genetic testing is particularly useful in cases where there is a suspected genetic cause for the condition, as it allows for the simultaneous analysis of multiple genes. This can help identify other genetic variants that may be contributing to the deficiency and provide a more comprehensive understanding of the underlying genetic factors involved.

Overall, NGS genetic testing of the NDUFAF1 gene can help diagnose mitochondrial complex I deficiency and provide valuable information for the management and treatment of affected individuals.

Test Name	NDUFAF1 Gene Mitochondrial complex I 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 NDUFAF1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF1 Gene Mitochondrial complex I deficiency
Test Details	The NDUFAF1 gene is responsible for encoding a protein that is involved in the assembly and stability of mitochondrial complex I, which is a crucial component of the mitochondrial respiratory chain. Mitochondrial complex I deficiency refers to a condition where there is a malfunction or deficiency in the function of this complex. NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the NDUFAF1 gene that may be responsible for the deficiency. By sequencing the DNA of an individual, NGS can identify specific genetic changes that may be affecting the function of the NDUFAF1 gene. This information can help diagnose mitochondrial complex I deficiency and guide treatment decisions. NGS genetic testing is particularly useful in cases where there is a suspected genetic cause for the condition, as it allows for the simultaneous analysis of multiple genes. This can help identify other genetic variants that may be contributing to the deficiency and provide a more comprehensive understanding of the underlying genetic factors involved. Overall, NGS genetic testing of the NDUFAF1 gene can help diagnose mitochondrial complex I deficiency and provide valuable information for the management and treatment of affected individuals.