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RTEL1 Gene Dyskeratosis Congenita Autosomal Recessive Type 5 Genetic Test

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

-21%

The “RTEL1 Gene Dyskeratosis Congenita Autosomal Recessive Type 5 Genetic Test” is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the RTEL1 gene, which are associated with Dyskeratosis Congenita, particularly the autosomal recessive type 5. Dyskeratosis Congenita (DC) is a rare, genetically inherited condition characterized by the premature aging of cells and tissues, leading to a wide range of clinical manifestations including skin abnormalities, nail dystrophy, oral leukoplakia, and a predisposition to bone marrow failure and cancer. The autosomal recessive type 5 variant of DC, linked to mutations in the RTEL1 gene, tends to present with similar but distinct features and may require specific management and treatment strategies.

This genetic test is critical for individuals suspected of having Dyskeratosis Congenita, especially when there is a family history or clinical symptoms suggestive of the RTEL1 gene involvement. Early and accurate diagnosis through this test can guide appropriate clinical management, surveillance for potential complications, and genetic counseling for affected families.

The test is performed at DNA Labs UAE, a facility known for its advanced genetic testing services. The cost of the test is 4400 AED, reflecting the specialized nature of the examination and the sophisticated technology employed in identifying the genetic alterations associated with this condition. By opting for this test, patients and their families can gain invaluable insights into their genetic health, empowering them with the information necessary to make informed decisions regarding their medical care and the management of Dyskeratosis Congenita.

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RTEL1 Gene Dyskeratosis Congenita Autosomal Recessive Type 5 Genetic Test

Genetic testing plays a crucial role in diagnosing and managing various genetic disorders. One such disorder is dyskeratosis congenita, autosomal recessive type 5, which is associated with the RTEL1 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, providing valuable insights into diagnosis and treatment options.

Test Details

The RTEL1 gene is linked to dyskeratosis congenita, a rare genetic disorder that affects multiple body systems, including the skin, nails, and bone marrow. Our Next-Generation Sequencing (NGS) technology allows us to analyze multiple genes simultaneously, providing a comprehensive evaluation of the RTEL1 gene.

Components and Price

The RTEL1 Gene Dyskeratosis Congenita Autosomal Recessive Type 5 Genetic Test is priced at AED 4400.0. The test requires a blood sample or extracted DNA, or a single drop of blood on an FTA card.

Report Delivery

After sample collection, the report will be delivered within 3 to 4 weeks. Our team of experts ensures accurate and timely reporting to facilitate prompt medical management.

Method

We utilize NGS technology for this genetic test. NGS is a cutting-edge sequencing technique that allows for the analysis of multiple genes simultaneously, providing comprehensive and accurate results.

Test Type

The RTEL1 Gene Dyskeratosis Congenita Autosomal Recessive Type 5 Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. Our dermatologists specialize in genetic testing and are well-equipped to handle this specific test.

Test Department and Doctor

This test is conducted under the Genetics department, and it is recommended to consult with a dermatologist for proper evaluation and guidance throughout the testing process.

Pre Test Information

Prior to the test, it is essential to provide the clinical history of the patient who is undergoing the RTEL1 Gene Dyskeratosis Congenita Autosomal Recessive Type 5 NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the RTEL1 gene.

Importance of Genetic Testing

Identifying mutations or variants in the RTEL1 gene through NGS genetic testing is crucial for diagnosing dyskeratosis congenita, autosomal recessive type 5. This information not only aids in determining appropriate medical management but also provides valuable insights for genetic counseling of affected individuals and their families.

It is important to note that dyskeratosis congenita is a complex disorder, and genetic testing may involve analyzing multiple genes associated with the condition, depending on the specific clinical presentation. Our healthcare professionals and genetic counselors are readily available to provide further information and guidance regarding NGS genetic testing for dyskeratosis congenita.

Test Name RTEL1 Gene Dyskeratosis congenita autosomal recessive type 5 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 RTEL1 Gene Dyskeratosis congenita, autosomal recessive type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RTEL1 Gene Dyskeratosis congenita, autosomal recessive type 5 NGS Genetic DNA Test gene RTEL1
Test Details

The RTEL1 gene is associated with a condition called dyskeratosis congenita, autosomal recessive type 5. Dyskeratosis congenita is a rare genetic disorder that affects multiple body systems, including the skin, nails, and bone marrow.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of dyskeratosis congenita, an NGS genetic test can analyze the RTEL1 gene to identify any disease-causing mutations or variants.

By identifying mutations in the RTEL1 gene, NGS genetic testing can help diagnose dyskeratosis congenita, autosomal recessive type 5. This information can be important for determining appropriate medical management and providing genetic counseling for affected individuals and their families.

It’s important to note that dyskeratosis congenita is a complex disorder, and genetic testing may involve analyzing multiple genes associated with the condition, depending on the specific clinical presentation. A healthcare professional or genetic counselor can provide more information and guidance regarding NGS genetic testing for dyskeratosis congenita.

SKU: TEST-2928 Category:

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