ENAM Gene Amelogenesis imperfecta type 1B Genetic Test
Welcome to DNA Labs UAE, where we offer the ENAM Gene Amelogenesis imperfecta type 1B Genetic Test. This genetic test is designed to identify mutations in the ENAM gene associated with Amelogenesis Imperfecta Type 1B (AI1B). AI1B is a genetic disorder that affects tooth enamel formation.
Test Components
The ENAM Gene Amelogenesis imperfecta type 1B Genetic Test includes:
- NGS Technology
Price
The cost of the ENAM Gene Amelogenesis imperfecta type 1B Genetic Test is 4400.0 AED.
Sample Condition
The test can be performed on the following sample conditions:
- Blood
- Extracted DNA
- One drop Blood on FTA Card
Report Delivery
The test results will be delivered within 3 to 4 weeks.
Method
The ENAM Gene Amelogenesis imperfecta type 1B Genetic Test utilizes NGS (Next-Generation Sequencing) technology.
Test Type
The test is categorized under Osteology, Dermatology, and Immunology Disorders.
Referring Doctor
The ENAM Gene Amelogenesis imperfecta type 1B Genetic Test is typically recommended by Dermatologists.
Test Department
This genetic test is conducted by our Genetics department.
Pre Test Information
Before undergoing the ENAM Gene Amelogenesis imperfecta type 1B Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by the ENAM Gene Amelogenesis imperfecta type 1B NGS Genetic DNA Test gene ENAM.
Test Details
The ENAM Gene Amelogenesis imperfecta type 1B Genetic Test is specifically designed to identify mutations in the ENAM gene associated with Amelogenesis Imperfecta Type 1B (AI1B). This test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes, including the ENAM gene, to detect any pathogenic mutations. By diagnosing AI1B and providing information about the specific genetic mutation present in an individual, this test can aid in treatment planning and genetic counseling.
It is important to note that this test focuses solely on the ENAM gene and is not a comprehensive genetic test for all types of Amelogenesis Imperfecta or other genetic conditions. It is typically recommended for individuals with suspected AI1B based on their clinical symptoms and family history. The test is performed on a blood or saliva sample, and the results are interpreted by a genetic specialist or healthcare provider.
| Test Name | ENAM Gene Amelogenesis imperfecta type 1B 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 ENAM Gene Amelogenesis imperfecta type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ENAM Gene Amelogenesis imperfecta type 1B NGS Genetic DNA Test gene ENAM |
| Test Details |
ENAM gene Amelogenesis imperfecta type 1B NGS Genetic Test is a genetic test that specifically looks for mutations in the ENAM gene associated with Amelogenesis Imperfecta Type 1B (AI1B). Amelogenesis Imperfecta (AI) is a group of genetic disorders that affect tooth enamel formation. AI1B is caused by mutations in the ENAM gene, which encodes for the enamelin protein involved in enamel development. The NGS (Next-Generation Sequencing) technique used in this test allows for the simultaneous analysis of multiple genes, including the ENAM gene, to identify any pathogenic mutations. This test can help diagnose AI1B and provide information about the specific genetic mutation present in an individual, which can aid in treatment planning and genetic counseling. It is important to note that this test specifically targets the ENAM gene and is not a comprehensive genetic test for all types of Amelogenesis Imperfecta or other genetic conditions. It is usually recommended for individuals with suspected AI1B based on their clinical symptoms and family history. The test is typically performed on a blood or saliva sample, and the results are interpreted by a genetic specialist or healthcare provider. |
