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MMP20 Gene Amelogenesis Imperfecta Type 2A2 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The MMP20 Gene Amelogenesis Imperfecta Type 2A2 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the MMP20 gene, which are associated with Amelogenesis Imperfecta (AI) Type 2A2. Amelogenesis Imperfecta is a genetic condition characterized by dental enamel defects, leading to abnormal tooth development, including issues with the color, thickness, and strength of enamel. The specific Type 2A2 variant of this condition implicates mutations in the MMP20 gene, which plays a crucial role in the proper development of enamel during tooth formation.

This genetic test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The test involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab, which is then analyzed in the lab to detect any mutations in the MMP20 gene. Identifying these mutations can confirm a diagnosis of Amelogenesis Imperfecta Type 2A2, enabling healthcare providers to offer appropriate treatment and management strategies for affected individuals.

The cost of the MMP20 Gene Amelogenesis Imperfecta Type 2A2 Genetic Test at DNA Labs UAE is 4400 AED. This price may cover the collection of the sample, the genetic analysis, and the provision of a detailed report explaining the test results. Patients and families opting for this test can gain valuable insights into the genetic underpinnings of their dental condition, paving the way for targeted interventions and improved dental care.

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  • This test is not intended for medical diagnosis or treatment
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MMP20 Gene Amelogenesis imperfecta type 2A2 Genetic Test

Are you or a family member affected by Amelogenesis imperfecta type 2A2? DNA Labs UAE offers the MMP20 Gene Amelogenesis imperfecta type 2A2 Genetic Test to help diagnose and manage this condition.

Test Details

The MMP20 gene is responsible for encoding an enzyme called matrix metalloproteinase-20, which plays a crucial role in tooth development. Mutations in this gene can lead to a condition called amelogenesis imperfecta (AI), specifically type 2A2. Amelogenesis imperfecta is a group of genetic disorders that affect the enamel formation of teeth. In type 2A2 AI, the enamel is typically hypoplastic, meaning it is thin and poorly mineralized. This can result in teeth that are discolored, rough, and prone to damage and decay.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the MMP20 gene. This test can identify mutations or variations in the MMP20 gene that may be associated with amelogenesis imperfecta type 2A2. By performing an NGS genetic test, healthcare professionals can diagnose individuals with amelogenesis imperfecta type 2A2 and provide appropriate management and treatment options. It can also help in identifying carriers of the condition within families and provide genetic counseling for future pregnancies.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on the individual’s specific situation.

Test Information

  • Test Name: MMP20 Gene Amelogenesis imperfecta type 2A2 Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 4400.0 AED
  • 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 MMP20 Gene Amelogenesis imperfecta type 2A2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MMP20 Gene Amelogenesis imperfecta type 2A2 NGS Genetic DNA Test gene MMP20

Conclusion

If you suspect you or a family member may have amelogenesis imperfecta type 2A2, consider getting the MMP20 Gene Amelogenesis imperfecta type 2A2 Genetic Test at DNA Labs UAE. This test can provide valuable insights into the genetic basis of the condition and help guide appropriate management and treatment options.

Test Name MMP20 Gene Amelogenesis imperfecta type 2A2 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 MMP20 Gene Amelogenesis imperfecta type 2A2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MMP20 Gene Amelogenesis imperfecta type 2A2 NGS Genetic DNA Test gene MMP20
Test Details

The MMP20 gene is responsible for encoding an enzyme called matrix metalloproteinase-20, which plays a crucial role in tooth development. Mutations in this gene can lead to a condition called amelogenesis imperfecta (AI), specifically type 2A2.

Amelogenesis imperfecta is a group of genetic disorders that affect the enamel formation of teeth. In type 2A2 AI, the enamel is typically hypoplastic, meaning it is thin and poorly mineralized. This can result in teeth that are discolored, rough, and prone to damage and decay.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the MMP20 gene. This test can identify mutations or variations in the MMP20 gene that may be associated with amelogenesis imperfecta type 2A2.

By performing an NGS genetic test, healthcare professionals can diagnose individuals with amelogenesis imperfecta type 2A2 and provide appropriate management and treatment options. It can also help in identifying carriers of the condition within families and provide genetic counseling for future pregnancies.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on the individual’s specific situation.