Primary Immunodeficiency tests in Dubai & UAE

Compare available Primary Immunodeficiency 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

950.00–2,800.00 AED

Clinical preparation

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Primary Immunodeficiency test prices

Showing 1–14 of 14 matching tests.

Primary Immunodeficiency diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4825 CD27 Gene Lymphoproliferative Syndrome Type 2 (CD27 Deficiency) Genetic Test This genetic test identifies pathogenic variants in the CD27 gene, confirming a diagnosis of Lymphoproliferative Syndrome Type 2 (CD27 Deficiency).	Peripheral Whole Blood or Saliva	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CD27 gene", "Coding region, exons, and splice sites"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected primary immunodeficiency", "Family history of CD27 deficiency", "Recurrent severe infections", "Chronic EBV viremia", "Lymphoma"] Measurement technique Confirm with laboratory Codes LOINC: 90377-2 ICD-10: D82.8 Clinical summary This genetic test identifies pathogenic variants in the CD27 gene, confirming a diagnosis of Lymphoproliferative Syndrome Type 2 (CD27 Deficiency).
TEST-4927 CD3D Gene Immunodeficiency Type 19 Genetic Test This genetic test identifies pathogenic variants in the CD3D gene associated with primary immunodeficiency type 19.	Whole blood (EDTA), extracted DNA, or FTA card blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CD3D gene sequence", "Copy Number Variations (CNVs) in CD3D gene"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical summary and family pedigree if available"] Indications ["Suspected primary immunodeficiency type 19", "Family history of CD3D-related immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 82936-5 ICD-10: D81.2 Clinical summary This genetic test identifies pathogenic variants in the CD3D gene associated with primary immunodeficiency type 19.
TEST-3381 CD79A Gene Agammaglobulinemia Type 3, Autosomal Recessive Genetic Test This genetic test analyzes the CD79A gene to detect mutations causing autosomal recessive agammaglobulinemia type 3.	2 mL EDTA whole blood or dried blood spot on FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CD79A gene sequence", "Pathogenic variants in CD79A"] Parameters [] Preparation ["No fasting required"] Indications ["Clinical suspicion of agammaglobulinemia", "Family screening following genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21659-9 ICD-10: D80.0 Clinical summary This genetic test analyzes the CD79A gene to detect mutations causing autosomal recessive agammaglobulinemia type 3.
TEST-4920 CTPS1 Gene Immunodeficiency Type 24 Genetic Test This genetic test identifies pathogenic variants in the CTPS1 gene, confirming a diagnosis of Immunodeficiency Type 24 (SCID).	Peripheral Whole Blood	12–16 business days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CTPS1 gene sequence", "Pathogenic variants in CTPS1"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session", "No fasting required"] Indications ["Suspected CTPS1-related SCID", "Family screening for CTPS1 variants", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 95271-6 ICD-10: D81.89 Clinical summary This genetic test identifies pathogenic variants in the CTPS1 gene, confirming a diagnosis of Immunodeficiency Type 24 (SCID).
TEST-3249 CYBA Gene (Chronic Granulomatous Disease, Autosomal Recessive, Cytochrome b-Negative) Genetic Test This genetic test identifies pathogenic variants in the CYBA gene associated with autosomal recessive Chronic Granulomatous Disease (CGD).	Peripheral whole blood (EDTA tube) or extracted DNA	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CYBA gene", "SNVs, indels, CNVs"] Parameters [] Preparation ["No specific fasting required", "Avoid sample collection during active systemic infection with fever >38.5°C"] Indications ["Suspected Chronic Granulomatous Disease (CGD)", "Family history of CGD", "Recurrent severe infections"] Measurement technique Confirm with laboratory Codes LOINC: 95150-7 ICD-10: D71 Clinical summary This genetic test identifies pathogenic variants in the CYBA gene associated with autosomal recessive Chronic Granulomatous Disease (CGD).
TEST-4923 GATA2 Gene Sequencing for Immunodeficiency Type 21 Test This test evaluates the GATA2 gene for mutations associated with Immunodeficiency Type 21 (MonoMAC syndrome).	Peripheral whole blood or dried blood spot (FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GATA2 gene mutations", "Diagnostic sensitivity for Immunodeficiency Type 21"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected Immunodeficiency Type 21 (MonoMAC syndrome)", "Family history of GATA2-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94241-3 ICD-10: D81.89 Clinical summary This test evaluates the GATA2 gene for mutations associated with Immunodeficiency Type 21 (MonoMAC syndrome).
TEST-543 IGHM Gene Agammaglobulinemia Type 1, Autosomal Recessive Genetic Test This test identifies pathogenic variants in the IGHM gene associated with autosomal recessive agammaglobulinemia type 1.	Peripheral whole blood (EDTA)	3–4 weeks (21–28 days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IGHM gene coding region", "Pathogenic variants"] Parameters [] Preparation ["No fasting or special diet required"] Indications ["Suspected autosomal recessive agammaglobulinemia type 1", "Family history of the disease"] Measurement technique Confirm with laboratory Codes LOINC: 33288-0 ICD-10: D80.0 Clinical summary This test identifies pathogenic variants in the IGHM gene associated with autosomal recessive agammaglobulinemia type 1.
TEST-4879 IL21R Gene Immunodeficiency, Primary, Autosomal Recessive, IL21R‑Related Genetic Test This test identifies pathogenic variants within the IL21R gene associated with autosomal recessive primary immunodeficiency.	Peripheral whole blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the IL21R gene", "Deletion/duplication analysis of the IL21R gene"] Parameters [] Preparation [] Indications ["Suspected autosomal recessive primary immunodeficiency", "Family history of IL21R-related immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 94223-5 ICD-10: D84.8 Clinical summary This test identifies pathogenic variants within the IL21R gene associated with autosomal recessive primary immunodeficiency.
TEST-5306 IL2RG Gene Combined Immunodeficiency, X-Linked, Moderate Test This test identifies pathogenic variants in the IL2RG gene associated with X-linked combined immunodeficiency, moderate form.	Peripheral Whole Blood, FTA Card, or Extracted DNA	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the IL2RG gene", "Entire coding region & splice sites"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Suspected X-linked combined immunodeficiency", "Family history of X-linked immunodeficiency", "Evaluation of primary immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: D81.2, Z00.5, D81.9 Clinical summary This test identifies pathogenic variants in the IL2RG gene associated with X-linked combined immunodeficiency, moderate form.
TEST-2401 Leucocyte Adhesion Deficiency (LAD I & II) Test This diagnostic test evaluates the expression levels of CD18 and CD15s proteins on leukocytes to diagnose Leucocyte Adhesion Deficiency (LAD I & II).	Peripheral whole blood (Lavender‑EDTA and Green‑Sodium Heparin)	Next Working Day (if sample received by 9 AM)	950.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CD18 expression on leukocytes", "CD15s expression on leukocytes"] Parameters [{"name": "CD18 Expression", "reference_range": null}, {"name": "CD15s Expression", "reference_range": null}] Preparation ["No specific fasting required.", "Avoid high-dose systemic corticosteroids (≥1 mg/kg/day) within 48 hours prior to blood draw."] Indications ["Suspected primary immunodeficiency", "Recurrent severe bacterial infections", "Delayed umbilical cord separation", "Unexplained neutrophilia in infants"] Measurement technique Confirm with laboratory Codes LOINC: 51785-5 ICD-10: D84.8 Clinical summary This diagnostic test evaluates the expression levels of CD18 and CD15s proteins on leukocytes to diagnose Leucocyte Adhesion Deficiency (LAD I & II).
TEST-5049 NCF2 Gene Chronic Granulomatous Disease Type 2 Genetic Test This test analyzes the NCF2 gene to detect mutations associated with Chronic Granulomatous Disease Type 2 (CGD). It identifies variants like SNVs, indels, and CNVs.	Whole Blood (Peripheral, EDTA) or FTA Card	3-4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NCF2 gene sequence", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation [] Indications ["Individuals with recurrent, severe bacterial or fungal infections", "Family history suggestive of X-linked or autosomal recessive CGD", "Unexplained granuloma formation", "Impaired NBT test results", "Carrier testing", "Preimplantation genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 91281-3 ICD-10: D71 Clinical summary This test analyzes the NCF2 gene to detect mutations associated with Chronic Granulomatous Disease Type 2 (CGD). It identifies variants like SNVs, indels, and CNVs.
TEST-4957 NFKB2 Gene Common Variable Immunodeficiency Type 10 (CVID10) Genetic Test This genetic test sequences the NFKB2 gene to identify pathogenic variants associated with Common Variable Immunodeficiency Type 10 (CVID10).	Whole Blood, Extracted DNA, or FTA Card Specimen	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NFKB2 gene sequence variants", "Copy Number Variations (CNVs) in NFKB2"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected Common Variable Immunodeficiency Type 10 (CVID10)", "Recurrent sinopulmonary infections", "Suspected pituitary hormone deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 76881-0 ICD-10: D83.8, D83.9 Clinical summary This genetic test sequences the NFKB2 gene to identify pathogenic variants associated with Common Variable Immunodeficiency Type 10 (CVID10).
TEST-4886 RORC Gene Immunodeficiency Type 42 Genetic Test This test sequences the RORC gene to identify variants associated with primary immunodeficiency type 42, a condition linked to recurrent fungal infections and autoimmune issues.	Whole blood (EDTA or FTA card) or extracted DNA	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic and likely pathogenic variants in the RORC gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number variants"] Parameters [] Preparation ["Do not discontinue prescribed antifungal or immunomodulatory therapy without consulting your referring physician", "Mandatory pre-test genetic counselling including construction of a three-generation pedigree", "Informed consent must be documented for all patients, with additional guardian consent for minors"] Indications ["Patients with recurrent fungal infections", "Patients with persistent dermatophyte infections", "Suspected Mendelian immunodeficiency involving the IL-17 immune axis"] Measurement technique Confirm with laboratory Codes LOINC: 95384-5 ICD-10: D84.8 Clinical summary This test sequences the RORC gene to identify variants associated with primary immunodeficiency type 42, a condition linked to recurrent fungal infections and autoimmune issues.
TEST-4569 ZAP70 Gene Selective T-cell Defect Genetic Test This test identifies pathogenic variants in the ZAP70 gene associated with severe combined immunodeficiency (SCID). It analyzes the full coding region and splice sites using Next G...	Peripheral Whole Blood	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ZAP70 gene", "Kinase activity disruption"] Parameters [] Preparation [] Indications ["Suspected SCID", "Family history of ZAP70 mutation", "Carrier screening for first-degree relatives of confirmed proband"] Measurement technique Confirm with laboratory Codes LOINC: 74698-1 ICD-10: D81.7 Clinical summary This test identifies pathogenic variants in the ZAP70 gene associated with severe combined immunodeficiency (SCID). It analyzes the full coding region and splice sites using Next Generation Sequencing.

Category overview

Primary Immunodeficiency: overview

Coping with unusually frequent, severe, or hard-to-treat infections demands a deep dive into your body’s foundational defense mechanisms to uncover the truth. Within our highly specialized Genetics services, Primary Immunodeficiency testing maps your DNA for inherited mutations that compromise normal immune system function. Utilizing cutting-edge sequencing technology, this precise molecular profiling helps identify subtle immunological defects, offering the critical clarity required to safely guide life-saving treatments, targeted antibody therapies, and specialized preventative care. Recognized for immunological diagnostic excellence among top diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, exceptional analytical accuracy, and highly efficient turnaround times. Protect your long-term health and resilience—schedule your primary immunodeficiency testing in UAE, arrange a comfortable home sample collection, or consult our dedicated immunology genetics experts.

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