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LAMA3 Gene Epidermolysis bullosa junctional Herlitz type Genetic Test Cost

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

-21%

The LAMA3 gene plays a critical role in the development and maintenance of the skin’s structural integrity. Mutations in this gene are associated with Junctional Epidermolysis Bullosa (JEB) of the Herlitz type, a severe genetic disorder characterized by blister formation within the skin and mucous membranes at sites of minor injury or friction. This condition is inherited in an autosomal recessive pattern, meaning that an affected individual must inherit two copies of the mutated gene, one from each parent, for the disease to manifest.

To diagnose this condition, genetic testing of the LAMA3 gene is available. This test is crucial for confirming the diagnosis, understanding the disease’s severity, and informing family planning decisions. In the United Arab Emirates, DNA Labs UAE offers this specific genetic test. The cost of the test is 4400 AED, a price that reflects the sophisticated technology and expertise required to accurately identify mutations in the LAMA3 gene. Conducted in a state-of-the-art laboratory by skilled geneticists, this test provides essential information for affected families, helping them navigate the challenges associated with Junctional Epidermolysis Bullosa Herlitz type.

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LAMA3 Gene Epidermolysis bullosa junctional Herlitz type Genetic Test

At DNA Labs UAE, we offer the LAMA3 Gene Epidermolysis bullosa junctional Herlitz type Genetic Test. This test is designed to diagnose a specific type of epidermolysis bullosa called junctional epidermolysis bullosa, Herlitz type (JEB-H).

Test Details

Junctional epidermolysis bullosa, Herlitz type (JEB-H) is a rare genetic disorder characterized by blistering and erosion of the skin and mucous membranes. The LAMA3 gene is associated with this condition.

Our LAMA3 Gene Epidermolysis bullosa junctional Herlitz type Genetic Test utilizes NGS (Next-Generation Sequencing) technology. NGS genetic testing allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of the LAMA3 gene.

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

Before undergoing the LAMA3 Gene Epidermolysis bullosa junctional Herlitz type Genetic Test, it is important to provide a clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the LAMA3 Gene Epidermolysis bullosa, junctional, Herlitz type NGS Genetic DNA Test gene LAMA3.

Benefits of NGS Genetic Testing

NGS genetic testing can help diagnose JEB-H and provide valuable information about the specific genetic changes responsible for the disease. This information can be used for genetic counseling, prenatal testing, and potentially developing targeted therapies or interventions for affected individuals.

Test Name LAMA3 Gene Epidermolysis bullosa junctional Herlitz type 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 LAMA3 Gene Epidermolysis bullosa, junctional, Herlitz type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LAMA3 Gene Epidermolysis bullosa, junctional, Herlitz type NGS Genetic DNA Test gene LAMA3
Test Details

The LAMA3 gene is associated with a specific type of epidermolysis bullosa called junctional epidermolysis bullosa, Herlitz type (JEB-H). This is a rare genetic disorder characterized by blistering and erosion of the skin and mucous membranes.

NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the case of JEB-H, NGS genetic testing can be used to identify mutations or variations in the LAMA3 gene that may be responsible for the development of the condition.

By analyzing the DNA sequence of the LAMA3 gene, NGS testing can help diagnose JEB-H and provide valuable information about the specific genetic changes that are causing the disease. This information can be used for genetic counseling, prenatal testing, and potentially developing targeted therapies or interventions for affected individuals.

SKU: TEST-2972 Category:

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