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ATP5F1A Gene Mitochondrial Complex V Deficiency Nuclear Type 4 Genetic Test Cost

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

-21%

The ATP5F1A Gene Mitochondrial Complex V Deficiency Nuclear Type 4 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE. This test is designed to identify mutations in the ATP5F1A gene, which are implicated in Mitochondrial Complex V Deficiency, Nuclear Type 4. This condition is a rare genetic disorder that affects the body’s ability to produce energy at the cellular level, leading to a range of symptoms that can include muscle weakness, neurological deficits, and developmental delays.

Mitochondrial Complex V, also known as ATP synthase, plays a crucial role in the final step of oxidative phosphorylation, where the majority of cellular ATP, the energy currency of the cell, is produced. Mutations in the ATP5F1A gene can impair the function of Complex V, resulting in reduced ATP production and the aforementioned symptoms.

The genetic test conducted at DNA Labs UAE involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific mutations in the ATP5F1A gene. This test is crucial for the accurate diagnosis of Mitochondrial Complex V Deficiency, Nuclear Type 4, and can provide essential information for managing the condition, including potential treatments and understanding the risk of passing the mutation to offspring.

The cost of the ATP5F1A Gene Mitochondrial Complex V Deficiency Nuclear Type 4 Genetic Test at DNA Labs UAE is 4400 AED. Given the complexity of the test and the specialized technology and expertise required to perform it, the cost reflects the comprehensive analysis and detailed report provided to patients and their healthcare providers. This test is a valuable tool for individuals and families seeking answers to unexplained symptoms related to energy metabolism disorders.

Description

ATP5F1A Gene Mitochondrial Complex V Deficiency Nuclear Type 4 Genetic Test

Test Name: ATP5F1A Gene Mitochondrial Complex V Deficiency Nuclear Type 4 Genetic Test

Components: ATP5F1A gene analysis

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 ATP5F1A Gene Mitochondrial Complex V Deficiency, Nuclear Type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ATP5F1A Gene Mitochondrial Complex V Deficiency, Nuclear Type 4.

Test Details:

ATP5F1A gene is associated with mitochondrial complex V deficiency, nuclear type 4. Mitochondrial complex V, also known as ATP synthase, is responsible for producing adenosine triphosphate (ATP), which is the main energy source for cells. A NGS (Next-Generation Sequencing) genetic test is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of ATP5F1A gene, NGS can be used to identify any genetic variations or mutations that may be present in the gene.

Mitochondrial complex V deficiency, nuclear type 4 is a rare genetic disorder characterized by a deficiency in the ATP5F1A gene, leading to impaired ATP production. This deficiency can result in a range of symptoms, including muscle weakness, developmental delays, intellectual disability, and other neurological problems.

NGS genetic testing for ATP5F1A gene can help diagnose individuals with mitochondrial complex V deficiency, nuclear type 4 by identifying any genetic variations or mutations in the gene. This can provide valuable information for patients and their healthcare providers, allowing for appropriate management and treatment strategies to be implemented.

It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics. They can provide personalized genetic counseling and guidance based on the test results.

Test Name	ATP5F1A Gene Mitochondrial complex V deficiency nuclear type 4 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 ATP5F1A Gene Mitochondrial complex V deficiency, nuclear type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ATP5F1A Gene Mitochondrial complex V deficiency, nuclear type 4
Test Details	ATP5F1A gene is associated with mitochondrial complex V deficiency, nuclear type 4. Mitochondrial complex V, also known as ATP synthase, is responsible for producing adenosine triphosphate (ATP), which is the main energy source for cells. A NGS (Next-Generation Sequencing) genetic test is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of ATP5F1A gene, NGS can be used to identify any genetic variations or mutations that may be present in the gene. Mitochondrial complex V deficiency, nuclear type 4 is a rare genetic disorder characterized by a deficiency in the ATP5F1A gene, leading to impaired ATP production. This deficiency can result in a range of symptoms, including muscle weakness, developmental delays, intellectual disability, and other neurological problems. NGS genetic testing for ATP5F1A gene can help diagnose individuals with mitochondrial complex V deficiency, nuclear type 4 by identifying any genetic variations or mutations in the gene. This can provide valuable information for patients and their healthcare providers, allowing for appropriate management and treatment strategies to be implemented. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics. They can provide personalized genetic counseling and guidance based on the test results.