What does Beta Thalassemia Prenatal Diagnosis measure?

Beta Thalassemia Prenatal Diagnosis test detects 97-99% of disease-causing as well as rare mutations in the HBB gene.

Why is Beta Thalassemia Prenatal Diagnosis done?

• To detect and diagnose beta thalassemia in unborn babies • To help parents make informed decisions about their pregnancy, assess the risk of passing on the disease, and plan for appropriate medical intervention or treatment, if necessary.

When is Beta Thalassemia Prenatal Diagnosis recommended and who should take the test?

Beta Thalassemia Prenatal Diagnosis is recommended under the following circumstances: • if one or both parents are known carriers of beta thalassemia • if there is a family history of beta thalassemia • if there is a previous child with beta-thalassemia • if either parent has a high risk of being a carrier based on their ethnic background • if prenatal screening tests indicate a high risk of having a baby with beta thalassemia

What if the results of the Beta Thalassemia Prenatal Diagnosis are abnormal?

Abnormal results suggest the presence of mutations associated with beta thalassemia.

What to expect during Beta Thalassemia Prenatal Diagnosis?

During the test, a sample of amniotic fluid or chorionic villus tissue is collected from the mother. A blood sample is also collected from the mother. The samples are sent to the laboratory for testing.

What preparations are required before Beta Thalassemia Prenatal Diagnosis?

• Provide a duly signed consent form as per PCPNDT guidelines, including a sample forwarding doctor's covering letter and Form G (for invasive techniques). • Ensure that clinical indication and family history information is provided. • Follow any specific instructions provided by your healthcare provider regarding fasting, medication, or other preparations. • Inform your doctor if you have any specific requirements.

What other tests may be ordered with Beta Thalassemia Prenatal Diagnosis?

• Complete Blood Count (CBC): This test measures the levels of different components in your blood and helps assess the severity of beta thalassemia. • Haemoglobin Electrophoresis: This test identifies abnormal types of haemoglobin, which can aid in the diagnosis and classification of beta thalassemia.

What is Beta Thalassemia Prenatal Diagnosis also known as?

24-hour urine 5-hydroxyindoleacetic acid test or 24-hour urine 5-HIAA test

What is beta thalassemia?

Beta thalassemia is an inherited blood disorder characterised by reduced or absent production of beta-globin protein, which is a component of haemoglobin. It leads to inadequate red blood cell production and can cause anaemia.

Beta Thalassemia Prenatal Diagnosis in Chennai

Also known as: Beta Thalassemia (Prenatal Testing ) - 30 Mutation Panel, Amniotic Fluid/EDTA Blood

50+ booked in last 3 days

No special precautions

Sample Type

Blood

Recommended for

Male, Female

Report

Within 24 Hours

Blood test at Home

NABL & CAP Accredited Labs

Accurate & Quality Test Reports

Trusted by Leading Doctors & Hospitals

Overview

Beta Thalassemia Prenatal Diagnosis is a specialized genetic test performed during pregnancy to identify hemoglobin variants and the most common sequence variants associated with beta thalassemia. This test detects 97-99% of disease-causing as well as rare mutations in the HBB gene, providing comprehensive coverage. Beta thalassemia is an inherited blood disorder characterized by reduced or absent production of beta-globin chains, resulting in abnormal hemoglobin production. The test is typically offered to couples who are carriers of beta thalassemia or have a family history of the condition. By analyzing a sample of fetal cells obtained through techniques such as chorionic villus sampling (CVS) or amniocentesis, this test allows for early detection and assessment of the risk of beta thalassemia, empowering parents to make informed decisions about their pregnancy and plan appropriate medical interventions or treatments for the affected child.

Beta Thalassemia (Prenatal Testing ) - 30 Mutation Panel, Amniotic Fluid/EDTA Blood Price in Chennai

Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Beta Thalassemia (Prenatal Testing ) - 30 Mutation Panel, Amniotic Fluid/EDTA Blood with a clear pricing structure

The price of Beta Thalassemia (Prenatal Testing ) - 30 Mutation Panel, Amniotic Fluid/EDTA Blood in Chennai is ₹ 17,655

We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.

Frequently Asked Questions

Why take Beta Thalassemia (Prenatal Testing ) - 30 Mutation Panel, Amniotic Fluid/EDTA Blood?

Is this test for you?

More Info on Beta Thalassemia (Prenatal Testing ) - 30 Mutation Panel, Amniotic Fluid/EDTA Blood

Ratings & Reviews (0)

No reviews available

Why Metropolis?

Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.

We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.