ERF Gene Craniosynostosis type 4 Genetic Test
Test Name: ERF Gene Craniosynostosis type 4 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 ERF Gene Craniosynostosis type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ERF Gene Craniosynostosis type 4 NGS Genetic DNA Test gene ERF
Test Details: The ERF gene is associated with Craniosynostosis type 4, which is a rare genetic disorder characterized by the premature fusion of certain skull bones in infancy. NGS (Next Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. An NGS genetic test for Craniosynostosis type 4 would involve sequencing the ERF gene to identify any mutations or variations that may be present. This can help in confirming a diagnosis and determining the specific genetic cause of the condition. Genetic testing can be beneficial for individuals with suspected or confirmed Craniosynostosis type 4, as it can provide important information about the underlying genetic cause, help guide treatment decisions, and provide valuable information for family planning. It is important to note that genetic testing for Craniosynostosis type 4 should be performed and interpreted by a qualified healthcare professional or genetic counselor, as they can provide appropriate counseling and guidance based on the results.
Test Name | ERF Gene Craniosynostosis 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 | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for ERF Gene Craniosynostosis type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ERF Gene Craniosynostosis type 4 NGS Genetic DNA Test gene ERF |
Test Details |
The ERF gene is associated with Craniosynostosis type 4, which is a rare genetic disorder characterized by the premature fusion of certain skull bones in infancy. NGS (Next Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. An NGS genetic test for Craniosynostosis type 4 would involve sequencing the ERF gene to identify any mutations or variations that may be present. This can help in confirming a diagnosis and determining the specific genetic cause of the condition. Genetic testing can be beneficial for individuals with suspected or confirmed Craniosynostosis type 4, as it can provide important information about the underlying genetic cause, help guide treatment decisions, and provide valuable information for family planning. It is important to note that genetic testing for Craniosynostosis type 4 should be performed and interpreted by a qualified healthcare professional or genetic counselor, as they can provide appropriate counseling and guidance based on the results. |