Hemoglobin D Punjab HbD Mutation Study Test sale cost 1200 AED
Beta Thalassemia Screening Prenatal Test sale cost 1450 AED Beta Thalassemia Screening Prenatal Test Cost 1,610 د.إ Original price was: 1,610 د.إ.1,450 د.إCurrent price is: 1,450 د.إ.
Warfarin Therapeutic Response Predictive Assay VKORC1 and CYP2C9 Test sale cost 1280 AED Warfarin Therapeutic Response Predictive Assay VKORC1 and CYP2C9 Test Cost 1,600 د.إ Original price was: 1,600 د.إ.1,280 د.إCurrent price is: 1,280 د.إ.
Sale!

Hemoglobin D Punjab HbD Mutation Study Test Cost

Original price was: 1,600 د.إ.Current price is: 1,200 د.إ.

-25%

The Hemoglobin D Punjab (HbD) Mutation Study Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to detect the presence of the HbD mutation, a variant form of hemoglobin. Hemoglobin is a protein in red blood cells responsible for carrying oxygen throughout the body. The HbD Punjab variant, also known as HbD Los Angeles or simply HbD, is one of the many hemoglobin variants that can affect the structure and function of hemoglobin. This particular variant is most commonly found in people of Punjabi descent but can occur in other populations as well.

The test is crucial for identifying individuals who carry the HbD mutation, as it can lead to conditions like hemoglobin D disease or, when combined with other hemoglobin mutations such as sickle cell trait, result in more severe disorders like sickle cell disease. Early detection through the Hemoglobin D Punjab HbD Mutation Study Test allows for appropriate genetic counseling and management strategies to mitigate health risks associated with the mutation.

Conducted at the state-of-the-art facilities of DNA Labs UAE, the test involves a simple blood draw from the patient. The sample is then analyzed using advanced genetic testing techniques to identify the presence of the HbD mutation. The cost of the test is 1200 AED, reflecting the sophisticated technology and expertise required to accurately detect and analyze the mutation.

Patients or individuals who suspect they might carry the mutation, or those with a family history of hemoglobin variants, are encouraged to consider this test. Early diagnosis can be essential in managing potential health issues and making informed decisions about family planning.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

Hemoglobin D Punjab (HbD) Mutation Study Test

Welcome to DNA Labs UAE, a leading genetic lab in the UAE. We offer a wide range of genetic tests, including the Hemoglobin D Punjab (HbD) Mutation Study Test. In this blog post, we will provide you with detailed information about this test, including its cost, symptoms, diagnosis, and more.

Test Name: Hemoglobin D Punjab (HbD) Mutation Study Test

Components:

  • Sterile container
  • Sterile Normal Saline Container
  • EDTA Vacutainer (2ml)

Price: 1200.0 AED

Sample Condition:

The Hemoglobin D Punjab (HbD) Mutation Study Test can be performed using amniotic fluid, chorionic villi, or cord blood as the sample.

Report Delivery: 7-8 days

Method: End Point PCR

Test Type: Genetics

Doctor: General Physician

Test Department:

Pre Test Information:

A prescription from a doctor is required to perform the Hemoglobin D Punjab (HbD) Mutation Study Test. However, the prescription is not applicable for surgery and pregnancy cases or for people planning to travel abroad.

Test Details

The Hemoglobin D Punjab (HbD) mutation is a genetic variant of hemoglobin, the protein responsible for carrying oxygen in red blood cells. This mutation is specific to the Punjab region in India. The HbD mutation is characterized by a single amino acid substitution in the beta-globin gene.

The normal hemoglobin molecule consists of two alpha-globin chains and two beta-globin chains. In individuals with the HbD mutation, the amino acid glutamic acid is replaced by glutamine at position 121 of the beta-globin chain. This mutation can lead to a variety of health effects, depending on the specific genetic background of the individual.

Some individuals may be asymptomatic carriers, meaning they have the mutation but do not experience any symptoms. Others may have mild to moderate symptoms, such as mild anemia or a slightly increased risk of blood clots. In rare cases, individuals with the HbD mutation may develop a condition called hemoglobin D disease, which is characterized by more severe symptoms including chronic anemia, jaundice, and an enlarged spleen.

Hemoglobin D disease is inherited in an autosomal recessive manner, meaning that both parents must carry the mutation for their child to be affected. Research on the HbD mutation has focused on understanding its molecular and cellular effects, as well as its clinical manifestations.

Studies have investigated the prevalence of the mutation in different populations, the molecular mechanisms underlying its effects on hemoglobin function, and the clinical management of individuals with HbD disease. Overall, the study of the HbD mutation has contributed to our understanding of the genetic basis of hemoglobin disorders and has implications for the diagnosis and treatment of affected individuals.

For more information about the Hemoglobin D Punjab (HbD) Mutation Study Test or to schedule an appointment, please contact DNA Labs UAE.

Test Name Hemoglobinb D PunjabHbD Mutation Study Test
Components Sterile container / Sterile Normal Saline Container / EDTA Vacutainer (2ml)
Price 1200.0 AED
Sample Condition Amniotic fluid \/ Chorionic villi \/ Cord blood
Report Delivery 7-8 days
Method End Point PCR
Test type Genetics
Doctor General Physician
Test Department:
Pre Test Information Hemoglobinb D Punjab(HbD) Mutation Study can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

The Hemoglobin D Punjab (HbD) mutation is a genetic variant of hemoglobin, the protein responsible for carrying oxygen in red blood cells. This mutation is specific to the Punjab region in India.

The HbD mutation is characterized by a single amino acid substitution in the beta-globin gene. The normal hemoglobin molecule consists of two alpha-globin chains and two beta-globin chains. In individuals with the HbD mutation, the amino acid glutamic acid is replaced by glutamine at position 121 of the beta-globin chain.

This mutation can lead to a variety of health effects, depending on the specific genetic background of the individual. Some individuals may be asymptomatic carriers, meaning they have the mutation but do not experience any symptoms. Others may have mild to moderate symptoms, such as mild anemia or a slightly increased risk of blood clots.

In rare cases, individuals with the HbD mutation may develop a condition called hemoglobin D disease, which is characterized by more severe symptoms including chronic anemia, jaundice, and an enlarged spleen. Hemoglobin D disease is inherited in an autosomal recessive manner, meaning that both parents must carry the mutation for their child to be affected.

Research on the HbD mutation has focused on understanding its molecular and cellular effects, as well as its clinical manifestations. Studies have investigated the prevalence of the mutation in different populations, the molecular mechanisms underlying its effects on hemoglobin function, and the clinical management of individuals with HbD disease.

Overall, the study of the HbD mutation has contributed to our understanding of the genetic basis of hemoglobin disorders and has implications for the diagnosis and treatment of affected individuals.

SKU: TEST-5359 Category:

Related products