SDHA Gene Leigh syndrome Genetic Test sale cost 4400 AED
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SDHA Gene Leigh syndrome Genetic Test

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

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The SDHA Gene Leigh Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the SDHA gene, which are associated with Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically emerges in the first year of life, characterized by progressive loss of mental and movement abilities. Mutations in the SDHA gene disrupt the function of the mitochondrial complex II, leading to this condition.

The test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific genetic mutations in the SDHA gene. This genetic test is crucial for early diagnosis, allowing for timely intervention and management of the syndrome.

DNA Labs UAE provides this comprehensive genetic testing service at a cost of 4400 AED. The test is conducted in their state-of-the-art facilities, ensuring accurate and reliable results. By identifying the genetic basis of Leigh syndrome, this test plays a vital role in the clinical management of affected individuals, offering insights into treatment options and prognosis.

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SDHA Gene Leigh Syndrome Genetic Test

Components: SDHA Gene Leigh syndrome 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 SDHA Gene Leigh syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SDHA Gene Leigh syndrome.

Test Details

The SDHA gene Leigh syndrome NGS genetic test is a type of genetic testing that focuses on the SDHA gene and its association with Leigh syndrome. Leigh syndrome is a rare inherited neurological disorder that typically begins in infancy or early childhood and is characterized by progressive loss of motor skills and cognitive decline.

The SDHA gene encodes a subunit of the succinate dehydrogenase enzyme complex, which is involved in the cellular energy production process. Mutations in the SDHA gene can disrupt the normal function of this enzyme complex, leading to the development of Leigh syndrome.

The NGS (Next-Generation Sequencing) technique used in this genetic test allows for the simultaneous analysis of multiple genes, including the SDHA gene, to identify any disease-causing mutations or variants. This method provides a more comprehensive and efficient approach to genetic testing compared to traditional sequencing methods.

The SDHA gene Leigh syndrome NGS genetic test can be used for diagnostic purposes in individuals suspected to have Leigh syndrome or for carrier testing in individuals with a family history of the condition. It can also be utilized for prenatal testing in families with a known SDHA gene mutation.

The results of this genetic test can help in confirming a diagnosis, guiding treatment decisions, providing information on disease prognosis, and informing reproductive planning for affected individuals and their families.

It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals with expertise in genetics.

Test Name SDHA Gene Leigh syndrome 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 SDHA Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SDHA Gene Leigh syndrome
Test Details

SDHA gene Leigh syndrome NGS genetic test is a type of genetic testing that focuses on the SDHA gene and its association with Leigh syndrome. Leigh syndrome is a rare inherited neurological disorder that typically begins in infancy or early childhood and is characterized by progressive loss of motor skills and cognitive decline.

The SDHA gene encodes a subunit of the succinate dehydrogenase enzyme complex, which is involved in the cellular energy production process. Mutations in the SDHA gene can disrupt the normal function of this enzyme complex, leading to the development of Leigh syndrome.

The NGS (Next-Generation Sequencing) technique used in this genetic test allows for the simultaneous analysis of multiple genes, including the SDHA gene, to identify any disease-causing mutations or variants. This method provides a more comprehensive and efficient approach to genetic testing compared to traditional sequencing methods.

The SDHA gene Leigh syndrome NGS genetic test can be used for diagnostic purposes in individuals suspected to have Leigh syndrome or for carrier testing in individuals with a family history of the condition. It can also be utilized for prenatal testing in families with a known SDHA gene mutation.

The results of this genetic test can help in confirming a diagnosis, guiding treatment decisions, providing information on disease prognosis, and informing reproductive planning for affected individuals and their families. It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals with expertise in genetics.

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