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ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test Cost

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

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The ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the ACVR2B gene, which are linked to the development of Heterotaxy Visceral Type 4. This condition is a rare congenital disorder characterized by the abnormal arrangement of the internal organs across the left-right axis of the body, potentially affecting the heart, liver, spleen, and intestines. Such anomalies can lead to complex health issues, necessitating early and accurate diagnosis.

Conducted at DNA Labs UAE, this genetic test provides a crucial insight into the genetic underpinnings of the disorder, enabling healthcare professionals to devise appropriate management and treatment plans for affected individuals. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the ACVR2B gene that are indicative of Heterotaxy Visceral Type 4.

The cost of the ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to detect the presence of genetic mutations associated with the condition, offering valuable information for affected individuals and their families. Early detection through this genetic test can significantly impact the clinical outcome, guiding interventions and potentially improving the quality of life for those with Heterotaxy Visceral Type 4.

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ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test

Welcome to DNA Labs UAE, where we offer the ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test. This test is designed to diagnose and provide medical management for individuals with the ACVR2B gene mutation associated with visceral heterotaxy type 4.

Test Details

The ACVR2B gene is responsible for producing a protein called activin receptor type-2B, which plays a crucial role in regulating cell development and differentiation in various tissues and organs. When this gene is mutated, it can lead to the abnormal arrangement of internal organs, known as heterotaxy. Visceral heterotaxy type 4 specifically affects the organs in the chest and abdomen.

Our ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test utilizes Next-Generation Sequencing (NGS) technology to analyze an individual’s DNA rapidly and comprehensively. By sequencing the ACVR2B gene, we can identify any variations or mutations that may be associated with the development of visceral heterotaxy type 4.

Test Components and Price

Test Name: ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test

Components: Blood Sample

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre-Test Information

Prior to the ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test, we recommend providing a clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by the ACVR2B gene mutation.

Benefits of the Test

By undergoing the ACVR2B Gene Heterotaxy Visceral Type 4 Genetic Test, individuals can receive a genetic diagnosis and access appropriate medical management and treatment options. This information is crucial for understanding the condition and providing personalized care.

At DNA Labs UAE, we prioritize accuracy, efficiency, and confidentiality. Our expert team of geneticists and healthcare professionals is dedicated to providing the highest quality genetic testing services.

Test Name ACVR2B Gene Heterotaxy visceral type 4 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ACVR2B Gene Heterotaxy, visceral type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACVR2B Gene Heterotaxy, visceral type 4 NGS Genetic DNA Test gene ACVR2B
Test Details

The ACVR2B gene is a gene that provides instructions for making a protein called activin receptor type-2B. This protein is involved in a signaling pathway that helps regulate the development and differentiation of cells in various tissues and organs.

Heterotaxy is a condition characterized by the abnormal arrangement or organization of the internal organs in the body. It can affect the heart, lungs, liver, spleen, and other organs. Visceral heterotaxy type 4 refers to a specific subtype of heterotaxy syndrome that is characterized by abnormalities in the organs located in the chest and abdomen.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the rapid and comprehensive analysis of a person’s DNA. It can detect variations or mutations in specific genes, including the ACVR2B gene, that may be associated with certain genetic conditions or diseases.

Therefore, an ACVR2B gene heterotaxy, visceral type 4 NGS genetic test would involve sequencing the ACVR2B gene to identify any variations or mutations that may be linked to the development of visceral heterotaxy type 4. This test can help provide a genetic diagnosis and guide appropriate medical management and treatment options for individuals with this condition.

SKU: TEST-4139 Category:

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