FGFR2 Gene Apert Syndrome Genetic Test
Components:
- Test Name: FGFR2 Gene Apert syndrome 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: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information:
Clinical History of Patient who is going for FGFR2 Gene Apert syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Apert syndrome NGS Genetic DNA Test gene FGFR2.
Test Details:
The FGFR2 gene is associated with a rare genetic disorder called Apert syndrome. Apert syndrome is characterized by craniosynostosis, which is the premature fusion of certain skull bones, leading to abnormal head shape and facial features. It also affects the hands and feet, causing fusion of certain fingers and toes.
NGS (Next-Generation Sequencing) genetic testing can be used to analyze the FGFR2 gene for mutations or variations that may be associated with Apert syndrome. This type of genetic testing allows for the simultaneous analysis of multiple genes or even the entire genome, providing a comprehensive assessment of genetic variants.
NGS genetic testing for Apert syndrome can help confirm a diagnosis, guide treatment decisions, and provide information for genetic counseling and family planning. It is typically performed on a blood or saliva sample and involves sequencing the DNA to identify any genetic changes in the FGFR2 gene.
It is important to note that genetic testing for Apert syndrome should be performed by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support.
| Test Name | FGFR2 Gene Apert syndrome 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 FGFR2 Gene Apert syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Apert syndrome NGS Genetic DNA Test gene FGFR2 |
| Test Details | The FGFR2 gene is associated with a rare genetic disorder called Apert syndrome. Apert syndrome is characterized by craniosynostosis, which is the premature fusion of certain skull bones, leading to abnormal head shape and facial features. It also affects the hands and feet, causing fusion of certain fingers and toes. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the FGFR2 gene for mutations or variations that may be associated with Apert syndrome. This type of genetic testing allows for the simultaneous analysis of multiple genes or even the entire genome, providing a comprehensive assessment of genetic variants. NGS genetic testing for Apert syndrome can help confirm a diagnosis, guide treatment decisions, and provide information for genetic counseling and family planning. It is typically performed on a blood or saliva sample and involves sequencing the DNA to identify any genetic changes in the FGFR2 gene. It is important to note that genetic testing for Apert syndrome should be performed by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support. |
