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IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 Genetic Test Cost

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

-21%

The IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the IBA57 gene. These mutations are associated with Multiple Mitochondrial Dysfunctions Syndrome Type 3 (MMDS3), a rare genetic disorder that impacts mitochondrial function, leading to a range of severe clinical manifestations, including neurological and developmental abnormalities.

This test is crucial for individuals suspected of having MMDS3, as it provides a definitive diagnosis by analyzing the genetic makeup of the patient for specific mutations in the IBA57 gene. Early and accurate diagnosis is essential for managing symptoms, potential interventions, and genetic counseling for affected families.

DNA Labs UAE, a leading facility in genetic testing, offers this comprehensive genetic test at a cost of 4400 AED. The test is conducted using advanced genomic technologies to ensure high accuracy and reliability of results, making it a valuable tool for affected individuals and their families seeking answers and options for managing this complex condition.

Description

IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 Genetic Test

Test Name: IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3.

Test Details:

The IBA57 gene is associated with a rare genetic disorder called multiple mitochondrial dysfunctions syndrome type 3. This syndrome is characterized by a wide range of symptoms that can vary in severity and presentation.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular disorder. In the case of IBA57 gene multiple mitochondrial dysfunctions syndrome type 3, NGS genetic testing can be used to identify mutations or variations in the IBA57 gene that may be causing the disorder.

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in the genes of interest. This can help in diagnosing the disorder, understanding its genetic basis, and providing appropriate management and treatment options.

It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS genetic testing for IBA57 gene multiple mitochondrial dysfunctions syndrome type 3, as well as to understand the potential benefits and limitations of the test.

Test Name	IBA57 Gene Multiple mitochondrial dysfunctions syndrome type 3 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 IBA57 Gene Multiple mitochondrial dysfunctions syndrome type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with IBA57 Gene Multiple mitochondrial dysfunctions syndrome type 3
Test Details	The IBA57 gene is associated with a rare genetic disorder called multiple mitochondrial dysfunctions syndrome type 3. This syndrome is characterized by a wide range of symptoms that can vary in severity and presentation. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular disorder. In the case of IBA57 gene multiple mitochondrial dysfunctions syndrome type 3, NGS genetic testing can be used to identify mutations or variations in the IBA57 gene that may be causing the disorder. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in the genes of interest. This can help in diagnosing the disorder, understanding its genetic basis, and providing appropriate management and treatment options. It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS genetic testing for IBA57 gene multiple mitochondrial dysfunctions syndrome type 3, as well as to understand the potential benefits and limitations of the test.