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RPL21 Gene Hypotrichosis type 12 Genetic Test Cost

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

-21%

The “RPL21 Gene Hypotrichosis Type 12 Genetic Test” is a specialized diagnostic assessment offered by DNA Labs UAE, designed to detect mutations in the RPL21 gene, which have been associated with Hypotrichosis Type 12. This condition is characterized by a scarcity of hair on the scalp and other parts of the body, often noticeable from birth. The test plays a crucial role in confirming the diagnosis, enabling healthcare providers to offer appropriate management strategies for affected individuals. With a cost of 4400 AED, this genetic test provides valuable insights into the genetic underpinnings of Hypotrichosis Type 12, facilitating personalized treatment plans and genetic counseling for families.

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RPL21 Gene Hypotrichosis type 12 Genetic Test

Welcome to DNA Labs UAE, where we offer the RPL21 Gene Hypotrichosis type 12 Genetic Test. This test is designed to identify any variations or mutations in the RPL21 gene that may be causing Hypotrichosis type 12, a rare genetic condition characterized by sparse or absent hair on the scalp and body.

Test Details

The RPL21 gene is associated with Hypotrichosis type 12. Our NGS (Next-Generation Sequencing) genetic testing method allows for the analysis of multiple genes simultaneously, providing a comprehensive understanding of an individual’s genetic makeup. By sequencing the RPL21 gene, we can identify any variations or mutations that could be causing the condition.

Test Components and Price

The RPL21 Gene Hypotrichosis type 12 Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or alternatively, one drop of blood on an FTA Card. The report delivery time is approximately 3 to 4 weeks.

Test Type and Doctor

The RPL21 Gene Hypotrichosis type 12 Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. It is performed by a Dermatologist in our Genetics department.

Pre Test Information

Prior to undergoing the RPL21 Gene Hypotrichosis type 12 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the RPL21 Gene Hypotrichosis type 12 NGS Genetic DNA Test gene RPL21.

Benefits of NGS Genetic Testing

NGS genetic testing is a powerful tool in the field of genetic medicine. It allows for the analysis of multiple genes at once, providing a more comprehensive understanding of an individual’s genetic makeup. In the case of Hypotrichosis type 12, NGS genetic testing can help confirm a diagnosis and provide information about the specific genetic cause of the disorder. This information can guide treatment decisions and provide insight into the likelihood of the condition being passed on to future generations.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to learn more about the RPL21 Gene Hypotrichosis type 12 Genetic Test and schedule an appointment.

Test Name RPL21 Gene Hypotrichosis type 12 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 RPL21 Gene Hypotrichosis type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RPL21 Gene Hypotrichosis type 12 NGS Genetic DNA Test gene RPL21
Test Details

RPL21 gene is associated with a rare genetic condition called Hypotrichosis type 12. Hypotrichosis refers to a condition characterized by sparse or absent hair on the scalp and body.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of genetic variations or mutations that may be responsible for a particular disorder or condition.

In the context of Hypotrichosis type 12, an NGS genetic test would involve sequencing the RPL21 gene to identify any variations or mutations that could be causing the condition. This test can help confirm a diagnosis and provide information about the specific genetic cause of the disorder.

NGS genetic testing is a powerful tool in the field of genetic medicine as it allows for the analysis of multiple genes at once, providing a more comprehensive understanding of an individual’s genetic makeup. It can also help guide treatment decisions and provide information about the likelihood of the condition being passed on to future generations.