Diagnostic options · UAE

Thalassemia tests in Dubai & UAE

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

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Listed price range

700.00–2,800.00 AED

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Thalassemia test prices

Showing 1–10 of 10 matching tests.

Thalassemia diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-526 Alpha Thalassemia HBA1–HBA2 Deletion‑Duplication Analysis Test This diagnostic test evaluates for large genetic rearrangements (deletions and duplications) within the HBA1 and HBA2 genes, which are the primary cause of alpha-thalassemia.	Whole blood (EDTA)	2–3 Weeks	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletions in HBA1 gene", "Duplications in HBA1 gene", "Deletions in HBA2 gene", "Duplications in HBA2 gene"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your physician.", "Results should be interpreted alongside complete blood count and hemoglobin electrophoresis."] Indications ["Suspected alpha-thalassemia", "Family screening for alpha-thalassemia", "Inconclusive results from other tests", "Pre-conception carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 42513-7 ICD-10: D56.0 Clinical summary This diagnostic test evaluates for large genetic rearrangements (deletions and duplications) within the HBA1 and HBA2 genes, which are the primary cause of alpha-thalassemia.
TEST-1809 Beta Thalassemia (9 Common Mutations) Screening Test This test identifies the presence of 9 common mutations associated with beta-thalassemia using molecular methods.	Peripheral whole blood	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Presence of specific beta-globin gene mutations"] Parameters [] Preparation ["No specific fasting required", "Inform the lab about any recent blood transfusions (within 12 weeks)"] Indications ["Carrier screening", "Preconception risk assessment", "Prenatal genetic counseling", "Individuals with unexplained microcytic anemia"] Measurement technique Confirm with laboratory Codes LOINC: 49519-1 ICD-10: Z13.0 Clinical summary This test identifies the presence of 9 common mutations associated with beta-thalassemia using molecular methods.
TEST-1810 Beta Thalassemia HBB Deletion/Duplication Analysis Test This diagnostic test evaluates the HBB gene for large deletions or duplications associated with beta-thalassemia syndromes.	Peripheral Whole Blood (standard); Cord Blood, Amniotic Fluid, Chorionic Villi (hospital collection required)	7–10 Business Days	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy number variations (deletions/duplications) in the HBB gene", "Presence of large genomic rearrangements"] Parameters [] Preparation ["Inform phlebotomist about anticoagulant, antiplatelet, or iron chelation therapy.", "Continue all prescribed medications unless directed otherwise by a specialist."] Indications ["Diagnostic confirmation of beta-thalassemia", "Family cascade screening", "Prenatal planning", "Identification of silent carriers", "Confirmation of hereditary persistence of fetal hemoglobin (HPFH)"] Measurement technique Confirm with laboratory Codes LOINC: 21665-2 ICD-10: D56.1 Clinical summary This diagnostic test evaluates the HBB gene for large deletions or duplications associated with beta-thalassemia syndromes.
TEST-1805 Beta Thalassemia HBB Full Gene Trio Analysis (Couple & Prenatal) Test This test evaluates the HBB gene in parents and fetus to detect pathogenic mutations associated with beta-thalassemia.	Peripheral blood (parents), Amniotic fluid, Chorionic villi, or Cord blood (fetus)	8–10 working days	2,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HBB gene sequence (coding and regulatory regions)", "Detection of pathogenic mutations"] Parameters [] Preparation [] Indications ["Couples with a family history of beta-thalassemia", "Consanguineous marriages", "Abnormal hemoglobin electrophoresis results", "Preconception risk assessment", "Prenatal decision-making", "Preimplantation genetic testing planning"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: D56.1, D56.3, Z14.8 Clinical summary This test evaluates the HBB gene in parents and fetus to detect pathogenic mutations associated with beta-thalassemia.
TEST-1812 Beta Thalassemia-9 Common Mutations Screening (Couple) Test This test identifies the presence of nine common beta-globin gene mutations in both partners to assess the risk of having a child with Beta Thalassemia Major.	Peripheral Blood (EDTA Whole Blood)	3–4 Days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Presence of nine common beta-globin gene mutations"] Parameters [] Preparation [] Indications ["Pre-conceptional carrier screening for couples", "Family planning in high-risk populations"] Measurement technique Confirm with laboratory Codes LOINC: 49213-7 ICD-10: D56.1 Clinical summary This test identifies the presence of nine common beta-globin gene mutations in both partners to assess the risk of having a child with Beta Thalassemia Major.
TEST-1649 Delta Beta-Thalassaemia Mutation Screening Test This diagnostic test evaluates for specific genetic mutations associated with delta and beta thalassaemia.	Peripheral Blood (Whole Blood)	3–4 Days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HBD gene mutations", "HBB gene mutations"] Parameters [] Preparation [] Indications ["Family history of thalassaemia", "Pre-surgical clearance", "Antenatal screening", "Mandatory travel medicals", "Diagnosis of thalassaemia intermedia", "Carrier status confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 49685-0 ICD-10: D56.8 Clinical summary This diagnostic test evaluates for specific genetic mutations associated with delta and beta thalassaemia.
TEST-3161 HBA1 Gene (Alpha Thalassemia) Genetic Test This test evaluates the entire coding region of the HBA1 gene for mutations, deletions, and copy-number variations associated with alpha-thalassemia.	Peripheral whole blood	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single-nucleotide variants (SNVs)", "Small insertion-deletions (indels)", "Large deletion/duplication events (CNVs)", "Copy Number Variations"] Parameters [] Preparation ["No fasting required", "Avoid blood transfusion within 14 days prior to sample collection"] Indications ["Carrier screening for reproductive planning", "Diagnosis of alpha-thalassemia syndromes", "Evaluation of unexplained anemia", "Pre-implantation genetic diagnosis (PGD) or prenatal diagnosis", "Family counselling"] Measurement technique Confirm with laboratory Codes LOINC: 92827-7 ICD-10: D56.0 Clinical summary This test evaluates the entire coding region of the HBA1 gene for mutations, deletions, and copy-number variations associated with alpha-thalassemia.
TEST-3262 Thalassemia Alpha Mutation Analysis Test This test identifies specific genetic mutations (deletions and point mutations) in the alpha globin genes (HBA1 and HBA2) responsible for alpha thalassemia.	Whole Blood (EDTA tube)	5 working days (Sample Mon by 9 AM → Report Fri)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletions in HBA1 gene", "Deletions in HBA2 gene", "Point mutations in HBA1 gene", "Point mutations in HBA2 gene"] Parameters [] Preparation ["No fasting required", "No medication changes required unless specified by doctor", "Complete Genomics Clinical Information Requisition Form (Form 20)"] Indications ["Diagnosis of alpha thalassemia syndromes", "Identification of alpha thalassemia carriers", "Genetic counseling for families with thalassemia", "Pre-marital screening", "Prenatal diagnosis support"] Measurement technique Confirm with laboratory Codes LOINC: 49685-6 ICD-10: D56.0 Clinical summary This test identifies specific genetic mutations (deletions and point mutations) in the alpha globin genes (HBA1 and HBA2) responsible for alpha thalassemia.
TEST-3254 Thalassemia Alpha Trio Prenatal Mutation Detection Test This test evaluates the presence and type of alpha-thalassemia mutations in the fetus, parents, and amniotic fluid.	Amniotic Fluid + Parental Peripheral Blood	5 Working Days	2,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Alpha-globin gene mutations", "Alpha-thalassemia deletions"] Parameters [] Preparation ["No specific patient preparation required for blood draw.", "Amniocentesis procedure performed by obstetrician."] Indications ["Parents are known or suspected carriers of alpha-thalassemia", "Previous child affected by alpha-thalassemia", "Abnormal prenatal ultrasound findings suggestive of anemia"] Measurement technique Confirm with laboratory Codes LOINC: 56913-4 ICD-10: D56.0, Z13.0, Z15.89 Clinical summary This test evaluates the presence and type of alpha-thalassemia mutations in the fetus, parents, and amniotic fluid.
TEST-3269 Thalassemia Beta Trio Prenatal Mutation Detection Test This test evaluates the beta-globin gene in the fetus and both parents to detect mutations associated with beta-thalassaemia.	Amniotic fluid (fetal) and EDTA whole blood (parents)	5 working days	2,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Beta-globin gene mutations", "Fetal genotype", "Parental carrier status"] Parameters [] Preparation ["Parents provide 4 mL EDTA whole blood each", "Amniotic fluid (10 mL) collected by obstetrician", "Samples must be shipped refrigerated (2-8°C); DO NOT FREEZE"] Indications ["Families at risk for beta-thalassaemia", "Prenatal genetic screening"] Measurement technique Confirm with laboratory Codes LOINC: 21698-3 ICD-10: D56.1, O35.8XX0, Z31.430 Clinical summary This test evaluates the beta-globin gene in the fetus and both parents to detect mutations associated with beta-thalassaemia.

Category overview

Thalassemia: overview

A family history of chronic anemia or unexplained fatigue warrants proactive, empowering insights to protect your health and confidently plan for your family's future. Integrated into our specialized Genetics and Hematology services, Thalassemia testing evaluates your carrier status and genetic risk for inherited blood disorders affecting hemoglobin production. By leveraging state-of-the-art diagnostic technology, this essential genetic profiling helps uncover underlying molecular risks, offering the critical data needed to safely guide personalized preventative care, hematological monitoring, and specialized reproductive counseling. Consistently trusted for wellness and family planning among the best diagnostic labs in Dubai and the UAE, DNA Labs is steadfastly committed to strict patient confidentiality, unparalleled analytical accuracy, and prompt, reliable reporting. Safeguard your family's hematological health—book your thalassemia testing in UAE, arrange a comfortable home sample collection, or connect with our dedicated wellness team.

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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.