AMBN Gene Amelogenesis imperfecta type 1F Genetic Test
Test Name: AMBN Gene Amelogenesis imperfecta type 1F Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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 AMBN Gene Amelogenesis imperfecta type 1F NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with AMBN Gene Amelogenesis imperfecta type 1F NGS Genetic DNA Test gene AMBN
Test Details:
AMBN gene Amelogenesis imperfecta type 1F NGS Genetic Test is a genetic test that analyzes the AMBN gene for mutations associated with Amelogenesis imperfecta type 1F. Amelogenesis imperfecta is a group of inherited disorders that affect the development of tooth enamel. Type 1F is a specific subtype caused by mutations in the AMBN gene. This gene provides instructions for making a protein called ameloblastin, which is involved in the formation of enamel.
The NGS (Next-Generation Sequencing) technique used in this test allows for the rapid and accurate analysis of the entire AMBN gene, enabling the detection of any disease-causing mutations. By identifying these mutations, healthcare professionals can provide a definitive diagnosis of Amelogenesis imperfecta type 1F and offer appropriate management and treatment options for affected individuals.
This genetic test is typically ordered by a healthcare provider specializing in genetics or dentistry. It involves collecting a sample of DNA, usually through a blood or saliva sample, and sending it to a laboratory for analysis. The results of the test can help confirm a diagnosis, provide information about the specific mutation, and guide treatment decisions.
It is important to note that genetic testing may have limitations, and the results should be interpreted by a healthcare professional familiar with the specific condition and the individual’s medical history. Genetic counseling may also be recommended to discuss the implications of the test results and provide support and guidance to individuals and their families.
| Test Name | AMBN Gene Amelogenesis imperfecta type 1F 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 AMBN Gene Amelogenesis imperfecta type 1F NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with AMBN Gene Amelogenesis imperfecta type 1F NGS Genetic DNA Test gene AMBN |
| Test Details |
AMBN gene Amelogenesis imperfecta type 1F NGS Genetic Test is a genetic test that analyzes the AMBN gene for mutations associated with Amelogenesis imperfecta type 1F. Amelogenesis imperfecta is a group of inherited disorders that affect the development of tooth enamel. Type 1F is a specific subtype caused by mutations in the AMBN gene. This gene provides instructions for making a protein called ameloblastin, which is involved in the formation of enamel. The NGS (Next-Generation Sequencing) technique used in this test allows for the rapid and accurate analysis of the entire AMBN gene, enabling the detection of any disease-causing mutations. By identifying these mutations, healthcare professionals can provide a definitive diagnosis of Amelogenesis imperfecta type 1F and offer appropriate management and treatment options for affected individuals. This genetic test is typically ordered by a healthcare provider specializing in genetics or dentistry. It involves collecting a sample of DNA, usually through a blood or saliva sample, and sending it to a laboratory for analysis. The results of the test can help confirm a diagnosis, provide information about the specific mutation, and guide treatment decisions. It is important to note that genetic testing may have limitations, and the results should be interpreted by a healthcare professional familiar with the specific condition and the individual’s medical history. Genetic counseling may also be recommended to discuss the implications of the test results and provide support and guidance to individuals and their families. |
