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BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test

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

-21%

The BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the BMPR2 gene, which are strongly associated with hereditary pulmonary arterial hypertension (PAH). This condition is characterized by high blood pressure in the arteries of the lungs, leading to heart failure if left untreated. The BMPR2 gene plays a crucial role in the development and function of blood vessels, and mutations in this gene can significantly increase an individual’s risk of developing PAH.

This test is particularly important for individuals with a family history of pulmonary hypertension, as it can provide vital information for early diagnosis and management of the condition. By identifying specific genetic mutations, healthcare providers can tailor treatment plans to manage symptoms effectively and potentially improve outcomes for patients with hereditary PAH.

The BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to interpret the results accurately. DNA Labs UAE utilizes state-of-the-art technology to ensure reliable and precise genetic testing, offering individuals and families critical insights into their genetic health and helping to guide clinical decision-making.

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  • This test is not intended for medical diagnosis or treatment
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BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test

At DNA Labs UAE, we offer the BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test. This test is designed to identify variations or mutations in the BMPR2 gene that may contribute to the development of primary pulmonary hypertension (PPH), also known as primary type pulmonary arterial hypertension (PAH).

Test Components and Price

The cost of the BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test is AED 4400.0. The test can be conducted using a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The report for the BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test will be delivered within 3 to 4 weeks.

Method

The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes. This enables the detection of variations or mutations associated with primary pulmonary hypertension.

Test Type and Doctor

The BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test falls under the category of Vascular Diseases. The test is conducted under the supervision of a General Physician in our Genetics department.

Pre Test Information

Prior to undergoing the BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test, it is essential 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 by primary pulmonary hypertension.

Test Details

Primary pulmonary hypertension is a rare and progressive disorder characterized by high blood pressure in the pulmonary arteries, which supply blood to the lungs. The BMPR2 gene is associated with this condition. NGS genetic testing is used to identify variations or mutations in the BMPR2 gene that may contribute to the development of primary pulmonary hypertension.

Genetic testing for BMPR2 gene mutations plays a crucial role in the diagnosis and management of primary pulmonary hypertension. It provides valuable information for patients and their families, helping them understand the disease better. The test can also identify individuals at risk of developing primary pulmonary hypertension, enabling early intervention and monitoring.

It is important to note that not all individuals with primary pulmonary hypertension will have a mutation in the BMPR2 gene. Other genetic and environmental factors may also contribute to the development of the condition. Therefore, it is recommended to consult with a healthcare professional or a genetic counselor to understand the implications of the test results.

Test Name BMPR2 Gene Pulmonary hypertension primary 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 Vascular Diseases
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for BMPR2 Gene Pulmonary hypertension, primary type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BMPR2 Gene Pulmonary hypertension, primary type NGS Genetic DNA Test gene BMPR2
Test Details

The BMPR2 gene is associated with primary pulmonary hypertension (PPH), also known as primary type pulmonary arterial hypertension (PAH). PPH is a rare, progressive disorder characterized by high blood pressure in the pulmonary arteries, which supply blood to the lungs.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and detect variations or mutations that may be associated with a particular condition. In the case of PPH, NGS genetic testing can be used to identify variations or mutations in the BMPR2 gene that may contribute to the development of the disease.

Genetic testing for BMPR2 gene mutations can help in the diagnosis of PPH and provide valuable information for patients and their families. It can also help identify individuals who may be at risk of developing PPH, allowing for early intervention and monitoring.

It is important to note that not all individuals with PPH will have a mutation in the BMPR2 gene, and not all individuals with a mutation in the BMPR2 gene will develop PPH. Other genetic and environmental factors may also contribute to the development of the condition.

If you are considering genetic testing for PPH, it is recommended to consult with a healthcare professional or a genetic counselor who can provide guidance and help you understand the implications of the test results.