MMP21 Gene Heterotaxy Visceral Type 7 Genetic Test sale cost 4400 AED
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MMP21 Gene Heterotaxy Visceral Type 7 Genetic Test Cost

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

-21%

The MMP21 Gene Heterotaxy Visceral Type 7 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the MMP21 gene that are associated with Heterotaxy Visceral Type 7. Heterotaxy syndrome is a rare congenital condition characterized by the abnormal arrangement of internal organs across the left-right axis of the body, which can affect the heart, liver, spleen, and intestines. This condition can lead to significant health issues, including complex heart defects, functional abnormalities, and potentially life-threatening complications.

The MMP21 gene plays a crucial role in the proper development of the body’s symmetry during the embryonic stage. Mutations in this gene can disrupt the normal left-right orientation, leading to the manifestations of heterotaxy syndrome. The genetic test involves analyzing the patient’s DNA to detect mutations in the MMP21 gene, providing vital information for diagnosis, management, and treatment planning for affected individuals and their families.

Offered at a cost of 4400 AED, the test at DNA Labs UAE represents an important step for families seeking answers to complex congenital conditions, enabling early intervention and personalized care strategies to manage the diverse challenges associated with Heterotaxy Visceral Type 7. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experienced geneticists, ensuring accurate and reliable test results for patients.

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  • This test is not intended for medical diagnosis or treatment
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MMP21 Gene Heterotaxy Visceral Type 7 Genetic Test

Are you looking for a reliable genetic lab in UAE for MMP21 Gene Heterotaxy Visceral Type 7 Genetic Test? Look no further than DNA Labs UAE. We offer comprehensive genetic testing services to help diagnose and understand genetic conditions.

Test Details

The MMP21 gene is a gene that encodes an enzyme called matrix metalloproteinase 21. This enzyme is involved in the breakdown of proteins in the extracellular matrix, which plays a role in tissue remodeling and development. Heterotaxy is a condition characterized by the abnormal arrangement of organs in the chest and abdomen. It is typically present from birth and can affect multiple organ systems, including the heart, lungs, liver, and intestines. Heterotaxy can lead to various health problems and may require surgical interventions. Visceral type 7 heterotaxy refers to a specific subtype of heterotaxy syndrome. It is characterized by specific patterns of organ arrangement and associated anomalies.

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

Before undergoing the MMP21 Gene Heterotaxy Visceral Type 7 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with MMP21 Gene Heterotaxy Visceral Type 7 NGS Genetic DNA Test gene MMP21.

About NGS Technology

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic mutations and alterations that may be associated with a particular condition or disease. Therefore, an NGS genetic test for MMP21 gene heterotaxy, visceral type 7 would involve sequencing the MMP21 gene and potentially other genes known to be associated with heterotaxy syndrome. The test aims to identify any genetic variations or mutations that may contribute to the development of the condition. This genetic information can be valuable for diagnosis, prognosis, and potentially guiding treatment decisions for individuals with heterotaxy syndrome. It can also provide valuable insights into the underlying molecular mechanisms of the condition.

Don’t wait any longer. Contact DNA Labs UAE today to schedule your MMP21 Gene Heterotaxy Visceral Type 7 Genetic Test. Early detection and diagnosis can make a significant difference in managing and treating genetic conditions.

Test Name MMP21 Gene Heterotaxy visceral type 7 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 MMP21 Gene Heterotaxy, visceral type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MMP21 Gene Heterotaxy, visceral type 7 NGS Genetic DNA Test gene MMP21
Test Details

The MMP21 gene is a gene that encodes an enzyme called matrix metalloproteinase 21. This enzyme is involved in the breakdown of proteins in the extracellular matrix, which plays a role in tissue remodeling and development.

Heterotaxy is a condition characterized by the abnormal arrangement of organs in the chest and abdomen. It is typically present from birth and can affect multiple organ systems, including the heart, lungs, liver, and intestines. Heterotaxy can lead to various health problems and may require surgical interventions.

Visceral type 7 heterotaxy refers to a specific subtype of heterotaxy syndrome. It is characterized by specific patterns of organ arrangement and associated anomalies.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic mutations and alterations that may be associated with a particular condition or disease.

Therefore, an NGS genetic test for MMP21 gene heterotaxy, visceral type 7 would involve sequencing the MMP21 gene and potentially other genes known to be associated with heterotaxy syndrome. The test aims to identify any genetic variations or mutations that may contribute to the development of the condition.

This genetic information can be valuable for diagnosis, prognosis, and potentially guiding treatment decisions for individuals with heterotaxy syndrome. It can also provide valuable insights into the underlying molecular mechanisms of the condition.

SKU: TEST-4142 Category:

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