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CALCRL Gene Vascular System Defects Due to CALCRL Deficiency Genetic Test Cost

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

-21%

The CALCRL gene plays a crucial role in the proper development and function of the vascular system. Mutations or deficiencies in the CALCRL gene can lead to a variety of vascular system defects, impacting blood flow and potentially leading to severe health issues. Recognizing the importance of early detection and management of CALCRL-related conditions, DNA Labs UAE offers a specialized genetic test designed to identify deficiencies in the CALCRL gene.

This genetic test is a vital tool for individuals with a family history of vascular system defects or those who have symptoms suggesting a potential CALCRL gene deficiency. By analyzing a sample of the patient’s DNA, the test can confirm whether there are mutations in the CALCRL gene that could contribute to vascular system abnormalities.

The cost of the CALCRL deficiency genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately assess the presence of CALCRL gene mutations. Given the complexity of genetic testing and the specialized analysis involved, the price reflects the meticulous process necessary to provide reliable results.

Undergoing this test at DNA Labs UAE ensures access to leading-edge genetic testing technology, expert analysis, and the potential to significantly impact patient care by guiding treatment decisions and preventive measures for those affected by or at risk of CALCRL-related vascular system defects.

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CALCRL Gene Vascular System Defects

Welcome to DNA Labs UAE, where we offer the CALCRL Gene Vascular System Defects Genetic Test. This test aims to identify any deficiencies in the CALCRL gene that may be causing vascular system defects. Read on to learn more about this test, its components, cost, symptoms, diagnosis, and more.

Test Name: CALCRL Gene Vascular System Defects Genetic Test

Components: CALCRL gene analysis

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: Next-Generation Sequencing (NGS) Technology

Test Type: Vascular Diseases

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Prior to undergoing the CALCRL Gene Vascular System Defects Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by CALCRL Gene Vascular System Defects.

Test Details

The CALCRL gene is responsible for encoding the calcitonin receptor-like receptor (CALCRL), which plays a crucial role in various physiological processes, including the regulation of blood vessel development and maintenance. Deficiencies in CALCRL can lead to vascular system defects.

The CALCRL Gene Vascular System Defects Genetic Test utilizes Next-Generation Sequencing (NGS) technology. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes or even the entire genome. It can identify genetic variations, such as mutations or deletions, in the CALCRL gene that may be responsible for vascular system defects.

By performing this genetic test, clinicians can accurately identify individuals with CALCRL deficiency, aiding in the diagnosis and management of vascular system defects. This information can be used to guide treatment decisions, provide genetic counseling, and potentially develop targeted therapies for individuals with CALCRL deficiency.

If you suspect a vascular system defect due to CALCRL deficiency, it is crucial to undergo the CALCRL Gene Vascular System Defects Genetic Test. Contact DNA Labs UAE today to schedule your test and gain valuable insights into your genetic makeup.

Test Name CALCRL Gene Vascular system defects due to CALCRL deficiency 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 Vascular Diseases
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CALCRL Gene Vascular system defects due to CALCRL deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CALCRL Gene Vascular system defects due to CALCRL deficiency NGS Genetic DNA Test gene CALCRL
Test Details

CALCRL gene is responsible for encoding the calcitonin receptor-like receptor (CALCRL), which is involved in various physiological processes, including the regulation of blood vessel development and maintenance. Deficiency in CALCRL can lead to vascular system defects, which can be identified using Next-Generation Sequencing (NGS) genetic testing.

NGS genetic testing is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. It can identify genetic variations, such as mutations or deletions, in the CALCRL gene that may be responsible for vascular system defects.

By performing NGS genetic testing, clinicians can identify individuals with CALCRL deficiency, which can help in the diagnosis and management of vascular system defects. This information can be used to guide treatment decisions, provide genetic counseling, and potentially develop targeted therapies for individuals with CALCRL deficiency.