FGFR2 Gene LADD Syndrome Genetic Test
Welcome to DNA Labs UAE, where we offer the FGFR2 Gene LADD Syndrome Genetic Test. This test is designed to diagnose and provide valuable information about LADD syndrome, a rare genetic disorder affecting multiple body systems.
Test Details
The FGFR2 gene is responsible for producing a protein called fibroblast growth factor receptor 2, which plays a crucial role in the development and maintenance of various tissues in the body, including the skeletal system, skin, and nervous system.
LADD syndrome, also known as lacrimo-auriculo-dento-digital syndrome, is caused by mutations in the FGFR2 gene. It is a rare genetic disorder that affects multiple body systems.
Our FGFR2 Gene LADD Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes. This advanced sequencing technology enables us to identify mutations in the FGFR2 gene and other related genes that may be responsible for the condition.
Test Components
- Test Name: FGFR2 Gene LADD 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
Prior to undergoing the FGFR2 Gene LADD Syndrome Genetic Test, it is important to provide the clinical history of the patient who will be tested. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the syndrome.
Benefits of the Test
By identifying specific mutations in the FGFR2 gene, our NGS genetic testing can confirm a diagnosis of LADD syndrome. This information is crucial for genetic counseling and managing the condition. Furthermore, the test can also help identify other affected family members who may be at risk of developing the syndrome.
At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. Our FGFR2 Gene LADD Syndrome Genetic Test can help you gain valuable insights into this rare genetic disorder. Contact us today to schedule an appointment.
Test Name | FGFR2 Gene LADD 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 LADD syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene LADD syndrome NGS Genetic DNA Test gene FGFR2 |
Test Details |
The FGFR2 gene is responsible for providing instructions to make a protein called fibroblast growth factor receptor 2. This protein is involved in the development and maintenance of various tissues in the body, including the skeletal system, skin, and nervous system. LADD syndrome, also known as lacrimo-auriculo-dento-digital syndrome, is a rare genetic disorder that affects multiple body systems. It is caused by mutations in the FGFR2 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of LADD syndrome, NGS genetic testing can be used to identify mutations in the FGFR2 gene and other related genes that may be responsible for the condition. By identifying specific mutations in the FGFR2 gene, NGS genetic testing can help confirm a diagnosis of LADD syndrome and provide valuable information for genetic counseling and management of the condition. It can also help identify other affected family members who may be at risk of developing the syndrome. |