Hemoglobinopathies tests in Dubai & UAE

Compare available Hemoglobinopathies tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

700.00–2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Hemoglobinopathies test prices

Showing 1–6 of 6 matching tests.

Hemoglobinopathies diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1859 Alpha Thalassemia Mutation Screening (3 Common Mutations) Test This test identifies the presence of three common alpha-globin gene mutations associated with alpha-thalassemia carrier status and disease.	Peripheral Whole Blood	7–8 working days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Presence of specific HBA1/HBA2 gene mutations", "Alpha-globin gene variant genotyping"] Parameters [] Preparation ["No fasting required", "Inform healthcare provider about medications/supplements"] Indications ["Carrier screening", "Diagnosis of alpha-thalassemia", "Pre-conception counselling", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 49273-9 ICD-10: D56.0 Clinical summary This test identifies the presence of three common alpha-globin gene mutations associated with alpha-thalassemia carrier status and disease.
TEST-3203 HBB Gene Sickle Cell Anemia Next-Generation Sequencing (NGS) Genetic Test This genetic test analyzes the HBB gene to detect mutations associated with sickle cell disease and trait.	Whole Blood (EDTA), Extracted DNA, or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HBB gene mutations (SNVs, Indels)", "Sickle cell disease variants"] Parameters [] Preparation ["Mandatory pre-test genetic counseling session", "Family pedigree chart documentation"] Indications ["Diagnosis of sickle cell disease", "Carrier screening", "Pre-transplant evaluation"] Measurement technique Confirm with laboratory Codes LOINC: 82916-7 ICD-10: D57.1, Z13.0 Clinical summary This genetic test analyzes the HBB gene to detect mutations associated with sickle cell disease and trait.
TEST-1541 Hemoglobin E (HbE) Mutation Screening Test This genetic test identifies the presence of the Hemoglobin E mutation in the HBB gene.	Peripheral Blood (Whole Blood)	3–4 Days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HBB gene point mutation (HbE variant)", "Carrier status for Hemoglobin E"] Parameters [] Preparation [] Indications ["Carrier screening", "Diagnosis of hemoglobinopathies", "Family planning", "Preoperative risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 49690-8 ICD-10: D57.4, Z13.0 Clinical summary This genetic test identifies the presence of the Hemoglobin E mutation in the HBB gene.
TEST-1516 Hereditary Persistence of Fetal Hemoglobin (HPFH) Genetic Test This genetic test identifies specific mutations or deletions in the beta-globin gene cluster associated with Hereditary Persistence of Fetal Hemoglobin (HPFH). It confirms the diag...	Amniotic fluid, Chorionic villi, Cord blood, Peripheral venous blood	7–8 Business Days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Beta-globin gene cluster mutations", "Large-scale deletions"] Parameters [] Preparation [] Indications ["Unexplained high HbF on electrophoresis/HPLC", "Prenatal diagnosis in families with known beta-globin mutations"] Measurement technique Confirm with laboratory Codes LOINC: 50542-7 ICD-10: D56.4 Clinical summary This genetic test identifies specific mutations or deletions in the beta-globin gene cluster associated with Hereditary Persistence of Fetal Hemoglobin (HPFH). It confirms the diagnosis and differentiates HPFH from other conditions causing elevated fetal hemoglobin.
TEST-3131 Sickle Cell Anemia Mutation Detection Test This test identifies specific DNA mutations in the HBB gene associated with sickle cell disease and related hemoglobinopathies.	Whole blood (4 mL, minimum 2 mL)	5 business days (sample Mon by 11 AM → report Friday)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the HBB gene", "Compound heterozygous states (e.g., HbC, HbD-Punjab, HbO-Arab)", "Silent carrier states"] Parameters [{"name": "HBB Gene Mutation Status", "reference_range": "Negative / Positive for specific mutations"}] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions (within 90 days)"] Indications ["Prenatal diagnosis", "Premarital genetic counseling", "Eligibility assessment for disease-modifying therapies", "Confirmation of sickle cell trait or disease", "Investigation of unexplained anemia"] Measurement technique Confirm with laboratory Codes LOINC: 34565-2 ICD-10: D57.1, D57.3 Clinical summary This test identifies specific DNA mutations in the HBB gene associated with sickle cell disease and related hemoglobinopathies.
TEST-1137 Sickle Cell Disease Mutation Screening Test This test identifies specific genetic mutations in the HBB gene associated with sickle cell disease and carrier status.	Peripheral Whole Blood (EDTA Tube)	3–4 Business Days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Point mutations in the HBB gene (HbS, HbC, HbE, β-thalassemia variants)", "Carrier status (heterozygous)", "Disease status (homozygous, compound heterozygous)"] Parameters [{"name": "HBB Gene Mutations", "reference_range": "Negative (Absence of tested mutations)"}] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Identification of sickle cell trait (HbAS)", "Diagnosis of sickle cell disease (HbSS, HbSC, HbSβ-thalassemia)", "Premarital screening", "Prenatal genetic assessment", "Pre-operative evaluation"] Measurement technique Confirm with laboratory Codes LOINC: 29697-3 ICD-10: Z13.0, D57.3 Clinical summary This test identifies specific genetic mutations in the HBB gene associated with sickle cell disease and carrier status.

Category overview

Hemoglobinopathies: overview

Dealing with severe fatigue, chronic anemia, or sudden pain crises requires highly rigorous diagnostic oversight to identify underlying inherited anomalies in your red blood cells. Integrated into our specialized Genetics and Hematology department, testing for Hemoglobinopathies evaluates your DNA to detect structural defects or production imbalances in your hemoglobin proteins. Utilizing state-of-the-art diagnostic technology, this expansive profiling delivers the critical clarity needed to diagnose complex conditions like beta-thalassemia or hemoglobin E disease, safely guiding your healthcare provider’s highly customized therapeutic strategies and long-term medical care. Widely respected for complex blood diagnostics among diagnostic labs in Dubai and the UAE, DNA Labs guarantees absolute patient confidentiality, unparalleled diagnostic precision, and highly efficient reporting for sensitive cases. Empower your customized medical journey—schedule your hemoglobinopathies testing in UAE, arrange a secure clinical sample collection, or reach out to our dedicated hematology specialists today.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.