NF2 Gene Neurofibromatosis Type 2 Genetic Test
Welcome to DNA Labs UAE, a leading genetic lab offering the NF2 Gene Neurofibromatosis Type 2 Genetic Test. In this blog, we will discuss the cost, symptoms, diagnosis, and other important details related to this test.
Test Name: NF2 Gene Neurofibromatosis Type 2 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: Cancer
- Doctor: Oncologist
- Test Department: Genetics
Pre Test Information:
Before undergoing the NF2 Gene Neurofibromatosis Type 2 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the NF2 gene.
Test Details:
Neurofibromatosis type 2 (NF2) is a rare genetic disorder that causes the growth of non-cancerous tumors in the nervous system, specifically in the brain and spinal cord. This disorder is caused by mutations in the NF2 gene, which produces a protein called merlin that regulates cell growth.
The NF2 Gene Neurofibromatosis Type 2 Genetic Test utilizes NGS (Next-Generation Sequencing) technology to identify mutations in genes associated with genetic disorders. In the case of NF2, this test analyzes the NF2 gene for any mutations or variations that may be present.
The NGS test for the NF2 gene involves obtaining a DNA sample, typically through a blood or saliva sample. The DNA is then sequenced using advanced technology that allows for the simultaneous analysis of multiple genes. This sequencing process helps identify any changes or variations in the NF2 gene sequence that may be responsible for causing NF2.
The results of the NGS genetic test can confirm a diagnosis of NF2 and provide valuable information for medical management and genetic counseling. It can also be used for carrier testing in individuals with a family history of NF2, as well as for prenatal testing in families at risk of having a child with NF2.
It is important to note that NGS genetic testing is a complex and specialized procedure that should be performed by a qualified genetic testing laboratory. The results should be interpreted by a healthcare professional trained in genetics to ensure accurate diagnosis and appropriate management of NF2.
At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. If you suspect NF2 or have a family history of the disorder, we recommend considering the NF2 Gene Neurofibromatosis Type 2 Genetic Test. Early detection and proper management can significantly improve the quality of life for individuals with NF2.
| Test Name | NF2 Gene Neurofibromatosis type 2 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 | Cancer |
| Doctor | Oncologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for NF2 Gene Neurofibromatosis type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NF2 Gene Neurofibromatosis type 2 NGS Genetic DNA Test gene NF2 |
| Test Details |
Neurofibromatosis type 2 (NF2) is a rare genetic disorder that causes the growth of non-cancerous tumors in the nervous system, particularly in the brain and spinal cord. It is caused by mutations in the NF2 gene, which is responsible for producing a protein called merlin that helps regulate cell growth. NGS (Next-Generation Sequencing) genetic testing is a method used to identify mutations in genes associated with genetic disorders. In the case of NF2, NGS testing can be used to analyze the NF2 gene for any mutations or variations that may be present. The NGS test for NF2 gene involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual undergoing testing. The DNA is then sequenced using advanced technology that allows for the simultaneous analysis of multiple genes. This sequencing process identifies any changes or variations in the NF2 gene sequence that may be responsible for causing NF2. The results of the NGS genetic test can help confirm a diagnosis of NF2 and provide valuable information for medical management and genetic counseling. It can also be used for carrier testing in individuals with a family history of NF2, as well as for prenatal testing in families at risk of having a child with NF2. It is important to note that NGS genetic testing is a complex and specialized procedure that should be performed by a qualified genetic testing laboratory. The results should be interpreted by a healthcare professional trained in genetics to ensure accurate diagnosis and appropriate management of NF2. |
