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LAMB3 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 LAMB3 gene is crucial for encoding the laminin-332 protein, which plays a significant role in anchoring the epidermis to the underlying dermis, thus ensuring skin integrity and strength. Mutations in the LAMB3 gene can lead to a severe form of Junctional Epidermolysis Bullosa (JEB), known as the Herlitz type. This genetic disorder is characterized by fragile skin that easily blisters and wounds, affecting both the skin and mucous membranes. It is a life-threatening condition often evident from birth.

To diagnose this condition accurately, genetic testing for mutations in the LAMB3 gene is essential. DNA Labs UAE offers a specialized test designed to identify these mutations, thereby confirming the diagnosis of Junctional Epidermolysis Bullosa Herlitz type. This test is critical for early intervention and management of the disease, providing essential information for genetic counseling and guiding treatment decisions.

The cost of the LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is conducted with high precision and accuracy, ensuring reliable results for affected families. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experienced professionals, ensuring that patients receive the highest standard of care and support throughout the testing process.

Home  Sample collection service available

  • 100% accuaret Test Results
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  • This test is not intended for medical diagnosis or treatment
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LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test

At DNA Labs UAE, we offer the LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test to help diagnose and provide valuable information about this rare genetic disorder.

Test Components

The LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test includes:

  • NGS Technology
  • Osteology Dermatology Immunology Disorders

Price

The cost of the LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test is 4400.0 AED.

Sample Condition

We accept the following sample conditions for the test:

  • Blood
  • Extracted DNA
  • One drop Blood on FTA Card

Report Delivery

The report for the LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test will be delivered within 3 to 4 weeks.

Method

The test is conducted using NGS (Next-generation sequencing) technology.

Test Type

The LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test is specifically designed for Osteology Dermatology Immunology Disorders.

Doctor

The test is recommended by dermatologists.

Test Department

The LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test is conducted in the Genetics department.

Pre Test Information

Prior to undergoing the LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type 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 by the LAMB3 Gene Epidermolysis Bullosa Junctional Herlitz Type Genetic Test gene LAMB3.

Test Details

The LAMB3 gene is associated with a rare genetic disorder called Epidermolysis Bullosa Junctional Herlitz Type (EB-H). This disorder affects the skin, making it extremely fragile and prone to blistering and erosions, often leading to serious complications.

Next-generation sequencing (NGS) technology is used in this genetic test to simultaneously analyze multiple genes, including the LAMB3 gene. By using NGS, variations or mutations in the LAMB3 gene that may be responsible for causing EB-H can be detected.

To perform the test, a sample of DNA is required. This can be obtained through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to identify any variations or mutations in the LAMB3 gene.

The results of the NGS genetic test provide valuable information about the specific genetic changes present in an individual with EB-H. This information can be used for diagnostic purposes, to confirm a suspected diagnosis of EB-H, and to provide genetic counseling to affected individuals and their families.

Please note that genetic testing for EB-H using NGS is typically conducted by specialized laboratories or genetic testing companies. It is recommended to consult with a healthcare professional or genetic counselor who can assist in the testing process and interpret the results.

Test Name LAMB3 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 LAMB3 Gene Epidermolysis bullosa, junctional, Herlitz type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LAMB3 Gene Epidermolysis bullosa, junctional, Herlitz type NGS Genetic DNA Test gene LAMB3
Test Details

The LAMB3 gene is associated with a rare genetic disorder called Epidermolysis bullosa, junctional, Herlitz type (EB-H). This disorder affects the skin, causing it to be extremely fragile and prone to blistering and erosions, often with serious complications.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the LAMB3 gene. NGS technology can detect variations or mutations in the LAMB3 gene that may be responsible for causing EB-H.

Genetic testing for EB-H using NGS involves obtaining a sample of DNA, typically through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to identify any variations or mutations in the LAMB3 gene.

The results of the NGS genetic test can provide valuable information about the specific genetic changes present in an individual with EB-H. This information can be used for diagnostic purposes, to confirm a suspected diagnosis of EB-H, and to provide genetic counseling to affected individuals and their families.

It is important to note that genetic testing for EB-H using NGS is typically performed by specialized laboratories or genetic testing companies. A healthcare professional or genetic counselor can help facilitate the testing process and interpret the results.

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