RAB23 Gene Carpenter Syndrome Genetic Test
Test Details
The RAB23 gene is associated with Carpenter syndrome, a rare genetic disorder characterized by craniofacial and skeletal abnormalities. This genetic test uses NGS (Next-Generation Sequencing) technology to analyze the RAB23 gene for mutations or variations that may be responsible for the disorder.
Test Components
- Price: 3200.0 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 RAB23 Gene Carpenter Syndrome NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the disorder.
Benefits of NGS Genetic Testing
NGS genetic testing allows for a more comprehensive and efficient analysis of multiple genes compared to traditional genetic testing methods. In the context of Carpenter syndrome, NGS genetic testing can provide valuable information about the presence of mutations in the RAB23 gene, aiding in diagnosis, genetic counseling, and potential treatment options.
Consultation
It is important to consult with a genetic counselor or healthcare provider to discuss the benefits, limitations, and potential risks associated with NGS genetic testing for Carpenter syndrome or any other genetic disorder.
Test Name | RAB23 Gene Carpenter syndrome Genetic Test |
---|---|
Components | |
Price | 3200.0 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 RAB23 Gene Carpenter syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB23 Gene Carpenter syndrome NGS Genetic DNA Test gene RAB23 |
Test Details |
The RAB23 gene is associated with Carpenter syndrome, which is a rare genetic disorder characterized by craniofacial abnormalities, such as a high forehead, wide-set eyes, and a flat nasal bridge, as well as other skeletal abnormalities, such as fused or missing fingers and toes. 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 Carpenter syndrome, NGS genetic testing can be used to identify mutations or variations in the RAB23 gene that may be responsible for the disorder. By analyzing the patient’s DNA, NGS genetic testing can provide valuable information about the presence of mutations in the RAB23 gene, which can help with diagnosis, genetic counseling, and potential treatment options. It allows for a more comprehensive and efficient analysis of multiple genes, compared to traditional genetic testing methods. It is important to consult with a genetic counselor or healthcare provider to discuss the benefits, limitations, and potential risks associated with NGS genetic testing for Carpenter syndrome or any other genetic disorder. |