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CEP290 Gene Meckel Syndrome Type 4 Genetic Test Cost

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

-21%

The CEP290 Gene Meckel Syndrome Type 4 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the CEP290 gene, which are linked to Meckel Syndrome Type 4. Meckel Syndrome is a rare genetic disorder characterized by kidney cysts, liver fibrosis, and brain anomalies, leading to a range of developmental issues. The CEP290 gene plays a crucial role in cellular structures that are essential for cell division and the development of many body organs.

This test is particularly valuable for families with a history of Meckel Syndrome or for individuals showing symptoms related to the disorder, as it can provide a definitive diagnosis. Early detection through genetic testing can aid in managing symptoms and improving the quality of life for those affected.

The cost of the CEP290 Gene Meckel Syndrome Type 4 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the detailed analysis required to detect any mutations in the CEP290 gene, providing essential information for diagnosis, treatment planning, and genetic counseling. Given the complexity and the specialized nature of this test, it is conducted with high precision and care, ensuring accurate and reliable results for patients and their families.

Description

CEP290 Gene Meckel Syndrome Type 4 Genetic Test

Test Name: CEP290 Gene Meckel Syndrome Type 4 Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Hepatology, Nephrology, Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for CEP290 Gene Meckel Syndrome Type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP290 Gene Meckel Syndrome Type 4 NGS Genetic DNA Test gene CEP290.

Test Details: The CEP290 gene is associated with Meckel Syndrome Type 4, which is a rare genetic disorder characterized by abnormalities in multiple organ systems, including the brain, kidneys, and liver. Meckel Syndrome Type 4 is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular condition. In the case of Meckel Syndrome Type 4, NGS genetic testing can be used to detect mutations in the CEP290 gene. This test can help confirm a diagnosis and provide information about the specific genetic mutation present, which can be useful for family planning and genetic counseling purposes.

It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Meckel Syndrome Type 4, as well as to understand the potential risks, benefits, and limitations of the test.

Test Name	CEP290 Gene Meckel syndrome type 4 Genetic Test
Components
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	Hepatology Nephrology Endocrinology Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for CEP290 Gene Meckel syndrome type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP290 Gene Meckel syndrome type 4 NGS Genetic DNA Test gene CEP290
Test Details	The CEP290 gene is associated with Meckel syndrome type 4, which is a rare genetic disorder characterized by abnormalities in multiple organ systems, including the brain, kidneys, and liver. Meckel syndrome type 4 is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the condition. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular condition. In the case of Meckel syndrome type 4, NGS genetic testing can be used to detect mutations in the CEP290 gene. This test can help confirm a diagnosis and provide information about the specific genetic mutation present, which can be useful for family planning and genetic counseling purposes. It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Meckel syndrome type 4, as well as to understand the potential risks, benefits, and limitations of the test.