PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 Genetic Test
Test Name: PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 NGS Genetic DNA Test gene PGAP2
Test Details: PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3 is a rare genetic disorder characterized by intellectual disability and elevated levels of alkaline phosphatase in the blood. It is caused by mutations in the PGAP2 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3, NGS genetic testing can be used to identify mutations in the PGAP2 gene that are responsible for the disorder. NGS genetic testing involves extracting DNA from a patient’s blood or saliva sample and then sequencing the DNA to identify any genetic variations or mutations. This can help in diagnosing the specific genetic cause of the disorder and providing information for genetic counseling and management of the condition. It is important to consult with a healthcare professional or genetic counselor to discuss the benefits, limitations, and implications of NGS genetic testing for PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3. They can provide guidance on the appropriateness of the test, potential risks, and available support services.
Test Name | PGAP2 Gene Hyperphosphatasia with mental retardation syndrome type 3 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 | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for PGAP2 Gene Hyperphosphatasia with mental retardation syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PGAP2 Gene Hyperphosphatasia with mental retardation syndrome type 3 NGS Genetic DNA Test gene PGAP2 |
Test Details |
PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3 is a rare genetic disorder characterized by intellectual disability and elevated levels of alkaline phosphatase in the blood. It is caused by mutations in the PGAP2 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3, NGS genetic testing can be used to identify mutations in the PGAP2 gene that are responsible for the disorder. NGS genetic testing involves extracting DNA from a patient’s blood or saliva sample and then sequencing the DNA to identify any genetic variations or mutations. This can help in diagnosing the specific genetic cause of the disorder and providing information for genetic counseling and management of the condition. It is important to consult with a healthcare professional or genetic counselor to discuss the benefits, limitations, and implications of NGS genetic testing for PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3. They can provide guidance on the appropriateness of the test, potential risks, and available support services. |