NF1 Gene Neurofibromatosis type 1 Genetic Test
Cost: AED 4400.0
Symptoms, Diagnosis, and Test Details
Neurofibromatosis type 1 (NF1) is a genetic disorder that causes tumors to grow on nerves throughout the body. It is caused by mutations in the NF1 gene, which provides instructions for producing a protein called neurofibromin. Neurofibromin helps regulate cell growth and division.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of the NF1 gene. This type of testing can identify specific mutations or changes in the gene that may be responsible for causing NF1.
The NGS genetic test for NF1 involves collecting a sample of DNA, usually through a blood sample or saliva sample. The DNA is then sequenced using advanced sequencing technology to analyze the entire NF1 gene. The results of the test can help confirm a diagnosis of NF1 and identify specific mutations within the gene.
Components and Test Information
- Test Name: NF1 Gene Neurofibromatosis type 1 Genetic Test
- Price: AED 4400.0
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Osteology Dermatology Immunology Disorders
- Doctor: Dermatologist
- Test Department: Genetics
- Pre Test Information: Clinical History of Patient who is going for NF1 Gene Neurofibromatosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NF1 Gene Neurofibromatosis type 1 NGS Genetic DNA Test gene NF1
Benefits of NGS Genetic Testing for NF1
NGS genetic testing for NF1 can be helpful in several ways. It can confirm a diagnosis in individuals with symptoms of NF1, but without a family history of the disorder. It can also provide information about the specific mutation(s) present in an individual, which can be useful for family planning and genetic counseling.
It’s important to note that while NGS genetic testing can provide valuable information, it may not detect all possible mutations in the NF1 gene. In some cases, additional testing methods may be necessary to fully evaluate the gene and confirm a diagnosis of NF1. It is recommended to consult with a genetic counselor or healthcare provider to discuss the best testing options for your specific situation.
| Test Name | NF1 Gene Neurofibromatosis type 1 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 | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for NF1 Gene Neurofibromatosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NF1 Gene Neurofibromatosis type 1 NGS Genetic DNA Test gene NF1 |
| Test Details |
Neurofibromatosis type 1 (NF1) is a genetic disorder that causes tumors to grow on nerves throughout the body. It is caused by mutations in the NF1 gene, which provides instructions for producing a protein called neurofibromin. Neurofibromin helps regulate cell growth and division. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of the NF1 gene. This type of testing can identify specific mutations or changes in the gene that may be responsible for causing NF1. The NGS genetic test for NF1 involves collecting a sample of DNA, usually through a blood sample or saliva sample. The DNA is then sequenced using advanced sequencing technology to analyze the entire NF1 gene. The results of the test can help confirm a diagnosis of NF1 and identify specific mutations within the gene. NGS genetic testing for NF1 can be helpful in several ways. It can confirm a diagnosis in individuals with symptoms of NF1, but without a family history of the disorder. It can also provide information about the specific mutation(s) present in an individual, which can be useful for family planning and genetic counseling. It’s important to note that while NGS genetic testing can provide valuable information, it may not detect all possible mutations in the NF1 gene. In some cases, additional testing methods may be necessary to fully evaluate the gene and confirm a diagnosis of NF1. It is recommended to consult with a genetic counselor or healthcare provider to discuss the best testing options for your specific situation. |
