Sale!

HBA1 Gene Thalassemia Alpha Genetic Test Cost

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

-21%

The HBA1 gene thalassemia alpha genetic test is a specialized diagnostic procedure designed to detect mutations in the HBA1 gene, which are responsible for alpha thalassemia, a genetic blood disorder. This condition affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. Mutations in the HBA1 gene can lead to various forms of alpha thalassemia, ranging from silent carriers with no apparent symptoms to more severe forms that can cause significant health issues, including anemia and complications in fetal development.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient’s DNA to identify mutations in the HBA1 gene. This information is crucial for diagnosing the specific type of alpha thalassemia, understanding the risk of transmitting the condition to offspring, and determining appropriate management and treatment plans for affected individuals.

The cost of the HBA1 gene thalassemia alpha genetic test at DNA Labs UAE is 4400 AED. This investment in health allows individuals and families to gain valuable insights into their genetic makeup, facilitating informed decisions about their healthcare and future family planning.

Description

HBA1 Gene Thalassemia alpha Genetic Test – DNA Labs UAE

Test Name: HBA1 Gene Thalassemia alpha Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test type: Hematology

Doctor: Hematologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for HBA1 Gene Thalassemia, alpha NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HBA1 Gene Thalassemia, alpha NGS Genetic DNA Test gene HBA1

Test Details: The HBA1 gene is responsible for producing one of the two types of alpha globin chains that make up hemoglobin, a protein in red blood cells that carries oxygen. Thalassemia is a group of inherited blood disorders characterized by abnormal production of hemoglobin. Thalassemia can result from mutations in the HBA1 gene, leading to reduced or absent production of alpha globin chains. This imbalance in globin chain production causes a disruption in the normal structure and function of hemoglobin, leading to various forms of thalassemia. Alpha NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool used to identify mutations in the HBA1 gene associated with thalassemia. This test involves sequencing the DNA of the HBA1 gene to detect any genetic variations or mutations that may be causing the disease. By identifying specific mutations in the HBA1 gene, alpha NGS genetic testing can help diagnose thalassemia and determine the severity of the condition. This information is crucial for genetic counseling, prenatal screening, and management of thalassemia patients.

Test Name	HBA1 Gene Thalassemia alpha 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	Hematology
Doctor	Hematologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for HBA1 Gene Thalassemia, alpha NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HBA1 Gene Thalassemia, alpha NGS Genetic DNA Test gene HBA1
Test Details	The HBA1 gene is responsible for producing one of the two types of alpha globin chains that make up hemoglobin, a protein in red blood cells that carries oxygen. Thalassemia is a group of inherited blood disorders characterized by abnormal production of hemoglobin. Thalassemia can result from mutations in the HBA1 gene, leading to reduced or absent production of alpha globin chains. This imbalance in globin chain production causes a disruption in the normal structure and function of hemoglobin, leading to various forms of thalassemia. Alpha NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool used to identify mutations in the HBA1 gene associated with thalassemia. This test involves sequencing the DNA of the HBA1 gene to detect any genetic variations or mutations that may be causing the disease. By identifying specific mutations in the HBA1 gene, alpha NGS genetic testing can help diagnose thalassemia and determine the severity of the condition. This information is crucial for genetic counseling, prenatal screening, and management of thalassemia patients.