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LRPPRC Gene Leigh syndrome French-Canadian type Genetic Test Cost

Name: LRPPRC Gene Leigh syndrome French-Canadian type Genetic Test Cost
SKU: TEST-1503
Price: 4400 AED
Availability: InStock

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

-21%

The LRPPRC gene Leigh syndrome French-Canadian type genetic test is a specialized diagnostic tool designed to identify mutations in the LRPPRC gene, which are responsible for causing Leigh syndrome French-Canadian type, a rare and severe neurological disorder. This genetic condition is particularly noted for its prevalence among the French-Canadian population of Quebec, but it can occur in other populations as well. Leigh syndrome is characterized by progressive loss of mental and movement abilities, leading to severe physical and neurological disabilities.

The test involves analyzing the patient’s DNA to detect specific mutations in the LRPPRC gene, which play a crucial role in cellular energy production. Identifying these mutations can confirm a diagnosis of Leigh syndrome French-Canadian type, enabling early intervention and management of the condition.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis with a focus on accuracy and reliability. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to perform this detailed genetic analysis. Early diagnosis through this test can significantly impact the management of the syndrome, allowing for tailored treatments and supportive care to improve the quality of life for affected individuals and their families.

Description

LRPPRC Gene Leigh Syndrome French-Canadian Type Genetic Test

Components: LRPPRC Gene Leigh syndrome French-Canadian type 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 LRPPRC Gene Leigh syndrome, French-Canadian type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LRPPRC Gene Leigh syndrome, French-Canadian type.

Test Details:

The LRPPRC gene is associated with Leigh syndrome, which is a rare genetic disorder characterized by progressive neurological degeneration. The French-Canadian type refers to a specific variant of Leigh syndrome that is more prevalent in the French-Canadian population.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular condition. In the case of LRPPRC gene Leigh syndrome, NGS genetic testing can be used to identify mutations in the LRPPRC gene that are responsible for causing the disorder.

NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in the LRPPRC gene. This can help in diagnosing Leigh syndrome and determining the specific genetic cause of the condition. It can also be used for carrier testing in individuals with a family history of Leigh syndrome to assess the risk of passing on the condition to their children.

It is important to consult with a genetic counselor or healthcare professional before undergoing any genetic testing. They can provide guidance on the appropriateness of the test, its potential benefits, limitations, and implications, as well as help interpret the results and provide appropriate counseling and support.

Test Name	LRPPRC Gene Leigh syndrome French-Canadian type 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 LRPPRC Gene Leigh syndrome, French-Canadian type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LRPPRC Gene Leigh syndrome, French-Canadian type
Test Details	The LRPPRC gene is associated with Leigh syndrome, which is a rare genetic disorder characterized by progressive neurological degeneration. The French-Canadian type refers to a specific variant of Leigh syndrome that is more prevalent in the French-Canadian population. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular condition. In the case of LRPPRC gene Leigh syndrome, NGS genetic testing can be used to identify mutations in the LRPPRC gene that are responsible for causing the disorder. NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in the LRPPRC gene. This can help in diagnosing Leigh syndrome and determining the specific genetic cause of the condition. It can also be used for carrier testing in individuals with a family history of Leigh syndrome to assess the risk of passing on the condition to their children. It is important to consult with a genetic counselor or healthcare professional before undergoing any genetic testing. They can provide guidance on the appropriateness of the test, its potential benefits, limitations, and implications, as well as help interpret the results and provide appropriate counseling and support.