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FOXRED1 Gene Mitochondrial Complex I Deficiency Genetic Test Cost

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

-21%

The FOXRED1 Gene Mitochondrial Complex I Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the FOXRED1 gene, which are associated with mitochondrial complex I deficiency. This condition is a rare genetic disorder that affects the mitochondrial respiratory chain, leading to a range of clinical manifestations including muscle weakness, heart disease, and neurological deficits. The test, priced at 4400 AED, involves analyzing the patient’s DNA to detect any genetic variations in the FOXRED1 gene that might disrupt the normal function of complex I, one of the key enzymes involved in cellular energy production. This precise genetic testing is crucial for confirming a diagnosis, guiding treatment options, and providing information on the risk of passing the condition to future generations. DNA Labs UAE employs advanced genetic testing technologies to ensure accurate and reliable results, supporting patients and their families in managing and understanding their genetic health.

Description

FOXRED1 Gene Mitochondrial complex I deficiency Genetic Test

Test Name: FOXRED1 Gene Mitochondrial complex I deficiency Genetic Test

Components: FOXRED1 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 FOXRED1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXRED1 Gene Mitochondrial complex I deficiency.

Test Details:

The FOXRED1 gene is responsible for encoding a protein called FOXRED1, which is involved in the assembly and function of mitochondrial complex I. Mitochondrial complex I is a large protein complex that plays a crucial role in the process of oxidative phosphorylation, which is responsible for generating energy in the form of ATP in the mitochondria.

Mutations in the FOXRED1 gene can lead to mitochondrial complex I deficiency, which is a rare genetic disorder characterized by a wide range of symptoms. These symptoms can include developmental delay, muscle weakness, seizures, intellectual disability, and various neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in the FOXRED1 gene, as well as other genes known to be associated with mitochondrial complex I deficiency.

By identifying the specific genetic mutations causing mitochondrial complex I deficiency, NGS genetic testing can help in the diagnosis and management of the condition. It can also provide valuable information for genetic counseling and family planning.

Test Name	FOXRED1 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 FOXRED1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FOXRED1 Gene Mitochondrial complex I deficiency
Test Details	The FOXRED1 gene is responsible for encoding a protein called FOXRED1, which is involved in the assembly and function of mitochondrial complex I. Mitochondrial complex I is a large protein complex that plays a crucial role in the process of oxidative phosphorylation, which is responsible for generating energy in the form of ATP in the mitochondria. Mutations in the FOXRED1 gene can lead to mitochondrial complex I deficiency, which is a rare genetic disorder characterized by a wide range of symptoms. These symptoms can include developmental delay, muscle weakness, seizures, intellectual disability, and various neurological problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in the FOXRED1 gene, as well as other genes known to be associated with mitochondrial complex I deficiency. By identifying the specific genetic mutations causing mitochondrial complex I deficiency, NGS genetic testing can help in the diagnosis and management of the condition. It can also provide valuable information for genetic counseling and family planning.