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COL4A2 Gene Porencephaly Type 2 Genetic Test Cost

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

-21%

The COL4A2 gene porencephaly type 2 genetic test is a specialized diagnostic tool designed to detect mutations in the COL4A2 gene, which are associated with porencephaly type 2, a rare neurological disorder. This condition is characterized by the presence of cysts or cavities within the cerebral hemispheres of the brain, leading to a range of symptoms such as developmental delay, seizures, and in some cases, hemiplegia (paralysis on one side of the body). The COL4A2 gene plays a crucial role in the formation and stability of blood vessels in the brain, and mutations in this gene can disrupt these processes, leading to the development of porencephaly.

The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics, offering a comprehensive range of genetic testing services. The cost of the COL4A2 gene porencephaly type 2 genetic test is 4400 AED. This test is particularly valuable for families with a history of the condition or for individuals presenting symptoms suggestive of porencephaly type 2. Early and accurate diagnosis through this genetic test can guide clinical management, inform prognosis, and assist in genetic counseling for affected families, helping them understand the risks of recurrence in future pregnancies.

Description

COL4A2 Gene Porencephaly type 2 Genetic Test

Components: COL4A2 Gene Porencephaly type 2 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 COL4A2 Gene Porencephaly type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL4A2 Gene Porencephaly type 2.

Test Details: The COL4A2 gene is responsible for providing instructions for making a protein called type IV collagen alpha-2 chain. This protein is a major component of basement membranes, which are thin, sheet-like structures that provide support and stability to tissues and organs. Porencephaly type 2 is a rare neurological disorder characterized by the presence of fluid-filled cavities or cysts in the brain. This condition is caused by mutations in the COL4A2 gene, which disrupt the normal production or structure of the type IV collagen alpha-2 chain protein. These mutations can lead to abnormalities in the development and maintenance of basement membranes in the brain, resulting in the formation of cysts. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and detect mutations or variations in their DNA sequences. In the case of COL4A2 gene porencephaly type 2, NGS genetic testing can be used to identify specific mutations or variations in the COL4A2 gene that are associated with this condition. This information can help with diagnosis, genetic counseling, and potentially guide treatment decisions.

Test Name	COL4A2 Gene Porencephaly type 2 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 COL4A2 Gene Porencephaly type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with COL4A2 Gene Porencephaly type 2
Test Details	The COL4A2 gene is responsible for providing instructions for making a protein called type IV collagen alpha-2 chain. This protein is a major component of basement membranes, which are thin, sheet-like structures that provide support and stability to tissues and organs. Porencephaly type 2 is a rare neurological disorder characterized by the presence of fluid-filled cavities or cysts in the brain. This condition is caused by mutations in the COL4A2 gene, which disrupt the normal production or structure of the type IV collagen alpha-2 chain protein. These mutations can lead to abnormalities in the development and maintenance of basement membranes in the brain, resulting in the formation of cysts. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and detect mutations or variations in their DNA sequences. In the case of COL4A2 gene porencephaly type 2, NGS genetic testing can be used to identify specific mutations or variations in the COL4A2 gene that are associated with this condition. This information can help with diagnosis, genetic counseling, and potentially guide treatment decisions.