Beta-thalassemia Screening by Thyrocare includes test on 5 parameters. It comprises of essential tests on Thalassemia for an early detection of any potential illness in your body. This package which comes under THALASSEMIA category , now available at a discounted price of Rs. 496
Beta-thalassemia Screening Info & Procedure
Group NameTHALASSEMIA
FastingFasting not required
Sample TypeEDTA
Sample CollectionExpert collect samples at Home
ReportsDelivered Online within 24-48 Hrs*
Report typeEmail & Hardcopy ( On request )
Tests included
5 parameters listed
Explore the tests in Beta-thalassemia Screening by category.
Thalassemia5
HEMOGLOBIN A2
HEMOGLOBIN C
HEMOGLOBIN D
HEMOGLOBIN F
HEMOGLOBIN S
Beta-thalassemia Screening Sample Report & Ranges
Conducted at
Thyrocare Labs
Lab Accreditation
CAP, NABL, ICMR, NGSP, ISO
Method
FULLY AUTOMATED HPLC USING BIO-RAD VARIANT II
TECHNOLOGY
H.P.L.C
Supervision
Dr Sachin Patil MD(Path)
Results
Highly Specific
Our labs work 365 days / 24 x 7 to ensure your Beta-thalassemia Screening samples reach us the same night, before midnight. We are equipped with (MUT) - India's first preanalytical barcoded vial sorter, Sample Sorter & Aptio (Siemens).
Our IT-enabled barcoded bi-directional operating systems & world-class air logistics process your blood samples within the specified time with the utmost accuracy. Once your specimen for Beta-thalassemia Screening is collected by our phlebotomist, Your reports will be sent to your email id within 24 to 48 hours. For hard copy requests, the reports would be delivered in 3 to 5 days. You will be informed via SMS & email once we process your report.
What to expect during a #testname# Blood Test?
During a #testname# blood test, a healthcare professional takes a blood sample from your arm, which is also known as venipuncture. A lab expert known as a phlebotomist conducts this process using a needle. He locates a vein on your arm and inserts the needle to draw blood. The blood sample will be transferred into a test tube and will be taken safely to the labs for the test.
The lab technicians will test the sample by following established standards, to ensure correct reports. Thyrocare Labs has a team of professionals who are skilled and experienced. After the testing is done, your reports are sent to your email within 1-2 days. On the other hand, if you need a hard copy of the report, expect the delivery of the same within 3-5 business days.
Preparations before a #testname# Blood Test?
For #testname# blood tests, special preparations are not needed. However, some important steps must be taken to ensure accuracy in the test reports.
#testname# test requires {[fasting]}, the same must be done for at least 8-10 hours. Only water can be consumed during this time. Being hydrated helps the blood draw easier and also ensures accurate results.
Eating junk food and consuming sweetened beverages or alcohol can alter your test results. So, it is advisable to be careful about what to consume or take the advice of a professional.
Consumption of certain medications is also prohibited before blood tests. You can discuss the details about the same with your doctor to be sure.
Avoid strenuous exercise as it can alter the readings of a blood test.
Are there any side effects of the test?
There are no side effects or risks attached to #testname# blood tests. The test involves the collection of a blood sample from your home. A phlebotomist draws blood from your arm using a needle, which only takes a few minutes. During this process, you might feel a sting on your arm, which is not painful. The blood sample will then be sent to the labs. Our medical experts take all precautions and safety measures during sample collection and testing.
Profile visual guide
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Beta-Thalassemia Screening Reference Guide
This profile reports five hemoglobin fractions: HbA2, HbC, HbD, HbF and HbS.
HbA2 and HbF can contribute to beta-thalassemia assessment, while HbC, HbD and HbS represent selected variants.
The package does not include a complete blood count, ferritin, iron studies, blood film or genetic testing.
A screening pattern must be interpreted with age, anemia findings, family history, pregnancy plans and recent transfusion history.
No fasting is required, but accurate clinical details are important before the report is interpreted.
Why This Test Is Ordered
Reason
Description
Understand the five reported fractions
HbA2 is a minor adult hemoglobin fraction containing delta globin chains.
HbF is fetal hemoglobin and normally predominates before birth.
HbC, HbD and HbS are selected structural hemoglobin variants.
The laboratory reports each named fraction as a separate result.
The five values form a pattern rather than five unrelated diagnoses.
HbA and HbE are not listed as separate results in this package.
CBC, ferritin, iron and molecular genetics are also not included.
Read the exact laboratory comments before assigning clinical meaning.
Use HbA2 as a screening clue
Raised HbA2 commonly supports consideration of beta-thalassemia carrier status.
The report-specific method and interval determine whether HbA2 is flagged.
HbA2 alone cannot establish the precise inherited beta-globin change.
Borderline values need red-cell indices, iron status and clinical context.
Iron deficiency can complicate interpretation of a possible carrier pattern.
Some hemoglobin variants can interfere with method-specific HbA2 measurement.
A normal-looking HbA2 does not exclude every thalassemia genotype.
Genetic testing may be appropriate when the clinical question remains unresolved.
Place HbF in age context
HbF carries oxygen during fetal life and falls after birth.
Infants naturally have more HbF than older children and adults.
Raised HbF in an adult can occur in several inherited conditions.
Beta-thalassemia patterns may include increased HbF alongside other findings.
HbF elevation is not specific enough to diagnose beta-thalassemia alone.
Pregnancy, treatment and selected blood disorders can alter HbF interpretation.
Age-specific laboratory guidance is essential for children and young infants.
Unexpected HbF should be reviewed with the complete hemoglobin pattern.
Recognise selected hemoglobin variants
HbS is associated with sickle-cell traits and diseases in different combinations.
HbC and HbD can also appear in carrier or compound patterns.
A detected fraction does not automatically distinguish trait from disease.
Relative proportions and companion fractions help define a likely pattern.
Some analytical methods cannot separate every variant with complete certainty.
An unexpected peak may need a second method or molecular confirmation.
Clinical severity cannot be predicted from one fraction percentage alone.
Specialist review is important when more than one variant is suspected.
Know what screening cannot prove
This profile is a screen for selected hemoglobin fractions, not complete genotyping.
Alpha-thalassemia can remain possible despite an unremarkable fraction pattern.
Silent or uncommon beta-globin changes may require molecular investigation.
The package cannot identify iron deficiency because ferritin is absent.
It cannot grade anemia because hemoglobin concentration and CBC are absent.
It cannot show red-cell size because MCV and MCH are not included.
A negative screen should not override a strong family or clinical history.
Further testing should answer the specific unresolved clinical question.
Symptoms And Who Should Test
Situation
Description
People planning a pregnancy
Carrier screening may be considered before pregnancy or early in pregnancy.
Testing before conception allows more time for informed reproductive decisions.
Hemoglobin traits can be present without symptoms or obvious anemia.
A carrier result should prompt appropriate testing of the reproductive partner.
When both partners carry relevant variants, genetic counselling clarifies inheritance risk.
This five-result profile does not replace comprehensive molecular carrier screening.
Previous reports should be reviewed before repeating tests during pregnancy.
An obstetric clinician can select pregnancy-appropriate confirmatory testing.
People with family history
A known family hemoglobin disorder can justify targeted laboratory assessment.
Bring the affected relative’s diagnosis or genetic report when available.
Family labels such as anemia may not identify the actual inherited condition.
The relevant variant determines which relatives and partners need testing.
An ordinary blood count cannot identify every hemoglobin carrier state.
A fraction screen may narrow the question without proving the genotype.
Genetics professionals can explain inheritance across parents, siblings and children.
Testing choices should reflect the documented family condition whenever possible.
People with microcytosis or anemia
Small red cells can occur with iron deficiency or thalassemia traits.
CBC indices provide essential context that this profile does not contain.
Ferritin helps assess iron stores when iron deficiency is clinically possible.
Empirical iron should not be started solely from a thalassemia suspicion.
Coexisting iron deficiency and a hemoglobin trait can complicate the pattern.
A blood film may add morphological information in selected anemia assessments.
Symptoms such as fatigue are too nonspecific to identify the cause.
Persistent anemia requires clinician-led evaluation beyond this screening profile.
People with an earlier abnormal screen
An earlier variant flag may require confirmation using another analytical method.
Bring the complete old report rather than recalling only a fraction name.
Why Choose Thyrocare for Beta-thalassemia Screening
Get tested for Beta-thalassemia Screening at fully automated diagnostic laboratory Thyrocare which has Centralized Processing Lab (CPL) for esoteric tests and Regional Processing Labs in major cities of India.
Home Based & Quality Diagnostics
at an Unbeatable Price
Carefully designed Panels to provide you with
the most vital information for your health.
Convenient Home Based
Affordable — Book Online
Certified Labs — NABL, CAP, ISO
Graphical Reports Online
Laboratory technology
Thyrocare Technologies Limited has huge set up covering over 2 Lakh sq. ft. floor area ensures zero error processing if approx 50 thousand specimens and over 3 lakh Clinical investigations per day is the right choice for your Beta-thalassemia Screening testing.