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MMP9 Gene Metaphyseal Anadysplasia Type 2 Genetic Test Cost

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

-21%

The MMP9 gene metaphyseal anadysplasia type 2 genetic test is a specialized diagnostic tool used to identify mutations in the MMP9 gene, which are linked to metaphyseal anadysplasia type 2, a rare genetic disorder. This condition is characterized by skeletal abnormalities including short stature, bowed legs, and other bone growth irregularities. The test is crucial for accurate diagnosis, enabling targeted treatment and management plans for affected individuals.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient’s DNA to look for specific mutations in the MMP9 gene that are known to cause the disorder. The process is comprehensive, ensuring a high degree of accuracy in the results.

The cost of the MMP9 gene metaphyseal anadysplasia type 2 genetic test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to conduct the test. Patients seeking this test can expect professional service and reliable results, providing crucial information for managing the condition effectively.

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MMP9 Gene Metaphyseal Anadysplasia Type 2 Genetic Test

At DNA Labs UAE, we offer the MMP9 Gene Metaphyseal Anadysplasia Type 2 Genetic Test. This test is designed to diagnose and provide valuable information about the rare genetic disorder known as metaphyseal anadysplasia type 2.

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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the MMP9 Gene Metaphyseal Anadysplasia 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 by the disorder.

Test Details

Metaphyseal anadysplasia type 2 (MMP9 gene) is a rare genetic disorder characterized by skeletal abnormalities, particularly in the metaphyses of long bones. This disorder is caused by mutations in the MMP9 gene, which encodes an enzyme called matrix metalloproteinase 9.

The NGS (Next-Generation Sequencing) genetic testing technique is used to analyze multiple genes, including the MMP9 gene. This technology allows for the rapid sequencing of large amounts of DNA, making it more efficient and cost-effective compared to traditional sequencing methods.

During the test, a DNA sample is obtained from the individual suspected of having metaphyseal anadysplasia type 2. This sample can be collected through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the MMP9 gene that may be responsible for the disorder.

The results of the NGS genetic test can confirm a diagnosis of metaphyseal anadysplasia type 2 and provide information about the specific genetic mutation present in the individual. This information is crucial for treatment decisions, genetic counseling, and family planning.

It is important to note that genetic testing should always be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Test Name MMP9 Gene Metaphyseal anadysplasia 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MMP9 Gene Metaphyseal anadysplasia type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MMP9 Gene Metaphyseal anadysplasia type 2 NGS Genetic DNA Test gene MMP9
Test Details

Metaphyseal anadysplasia type 2 (MMP9 gene) is a rare genetic disorder characterized by skeletal abnormalities, particularly in the metaphyses of long bones. It is caused by mutations in the MMP9 gene, which encodes an enzyme called matrix metalloproteinase 9.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the MMP9 gene. This technique uses high-throughput sequencing technology to rapidly sequence large amounts of DNA, making it more efficient and cost-effective compared to traditional sequencing methods.

NGS genetic testing for metaphyseal anadysplasia type 2 involves obtaining a DNA sample, typically through a blood sample or cheek swab, from the individual suspected of having the disorder. The DNA is then sequenced using NGS technology to identify any mutations or variations in the MMP9 gene that may be responsible for the condition.

The results of the NGS genetic test can help confirm a diagnosis of metaphyseal anadysplasia type 2 and provide information about the specific genetic mutation present in the individual. This information can be used to guide treatment decisions and provide valuable information for genetic counseling and family planning.

It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

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