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ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 Genetic Test Cost

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

-21%

The ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to detect mutations in the ISCA2 gene. These mutations are associated with Multiple Mitochondrial Dysfunctions Syndrome Type 4, a rare genetic condition that affects mitochondrial function, leading to a range of symptoms including developmental delay, muscle weakness, and metabolic abnormalities. The test is crucial for early diagnosis and management of the condition. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately identify the genetic alterations in the ISCA2 gene. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test represents a significant step forward in the genetic diagnosis and personalized medicine for patients with suspected mitochondrial disorders.

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ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 Genetic Test

At DNA Labs UAE, we offer the ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 Genetic Test. This test is designed to diagnose a rare genetic disorder that affects the function of mitochondria, the energy-producing structures within cells.

Test Components and Price

The ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 Genetic Test is priced at 4400.0 AED. The test requires a blood or extracted DNA sample, or one drop of blood on an FTA card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously.

Test Type and Doctor

The ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 Genetic Test falls under the category of Neurological Disorders. It is recommended to consult with a Neurologist for this test.

Test Department and Pre Test Information

The test is conducted in the Genetics department. Before undergoing the ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the syndrome.

Test Details

The ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 is a rare genetic disorder caused by mutations in the ISCA2 gene. This gene is involved in the assembly of iron-sulfur clusters, which are important components of many proteins involved in various cellular processes.

An NGS genetic test is used to identify mutations in the ISCA2 gene, allowing for a diagnosis of the syndrome. The test involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DNA to identify any mutations or changes in the ISCA2 gene.

The results of the test can confirm a diagnosis of ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 and provide information about the specific genetic mutation present in an individual.

It is important to note that genetic testing for ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 may not be available at all healthcare facilities. The decision to undergo genetic testing should be made in consultation with a healthcare professional or genetic counselor.

Test Name ISCA2 Gene Multiple mitochondrial dysfunctions syndrome 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 ISCA2 Gene Multiple mitochondrial dysfunctions syndrome type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ISCA2 Gene Multiple mitochondrial dysfunctions syndrome type 4
Test Details

ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 is a rare genetic disorder that affects the function of mitochondria, which are the energy-producing structures within cells. This syndrome is caused by mutations in the ISCA2 gene, which is involved in the assembly of iron-sulfur clusters, important components of many proteins involved in various cellular processes.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4, an NGS genetic test can be used to identify mutations in the ISCA2 gene, allowing for a diagnosis of the syndrome.

This genetic test involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DNA to identify any mutations or changes in the ISCA2 gene. The results of the test can help confirm a diagnosis of ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 and provide information about the specific genetic mutation present in an individual.

It is important to note that genetic testing for ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 may not be available at all healthcare facilities, and the decision to undergo genetic testing should be made in consultation with a healthcare professional or genetic counselor.

SKU: TEST-1742 Category:

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