Hemophagocytic Lymphohistiocytosis tests in Dubai & UAE

Compare available Hemophagocytic Lymphohistiocytosis 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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2,800.00 AED

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Hemophagocytic Lymphohistiocytosis test prices

Showing 1–4 of 4 matching tests.

Hemophagocytic Lymphohistiocytosis diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5062 PRF1 Gene NGS Test for Hemophagocytic Lymphohistiocytosis Type 2 This test evaluates the PRF1 gene for pathogenic variants associated with familial hemophagocytic lymphohistiocytosis type 2 (FHL2).	Whole blood, extracted DNA, 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 ["Pathogenic variants in the PRF1 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required.", "Inform provider of any recent blood transfusions.", "Mandatory genetic counseling required before testing."] Indications ["Suspected familial hemophagocytic lymphohistiocytosis type 2 (FHL2)", "Family history of FHL2", "Evaluation of severe, unexplained immune dysregulation"] Measurement technique Confirm with laboratory Codes LOINC: 83267-1 ICD-10: D76.1 Clinical summary This test evaluates the PRF1 gene for pathogenic variants associated with familial hemophagocytic lymphohistiocytosis type 2 (FHL2).
TEST-5057 STX11 Gene Hemophagocytic Lymphohistiocytosis Type 4 (FHL4) Genetic Test This test analyzes the STX11 gene for mutations associated with Familial Hemophagocytic Lymphohistiocytosis Type 4 (FHL4). It identifies pathogenic variants to confirm diagnosis an...	Peripheral Whole Blood or Buccal Swab	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic mutations in the STX11 gene", "Copy number variations (deletions/duplications) in the STX11 gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected primary HLH cases", "Individuals with symptoms suggestive of FHL4", "Carrier screening in families with known STX11 mutations", "Evaluation of asymptomatic siblings in affected families"] Measurement technique Confirm with laboratory Codes LOINC: 94533-7 ICD-10: D76.1 Clinical summary This test analyzes the STX11 gene for mutations associated with Familial Hemophagocytic Lymphohistiocytosis Type 4 (FHL4). It identifies pathogenic variants to confirm diagnosis and guide management.
TEST-5025 STXBP2 Gene Hemophagocytic Lymphohistiocytosis Type 5 Genetic Test This genetic test identifies pathogenic variants in the STXBP2 gene associated with Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL5).	Whole Blood (EDTA tube, 3–5 mL), Extracted DNA (≥1 µg at ≥50 ng/µL), 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 ["STXBP2 gene sequence", "Pathogenic variants in STXBP2"] Parameters [] Preparation ["Clinical history documentation", "Genetic counselling session with pedigree chart"] Indications ["Suspected Familial Hemophagocytic Lymphohistiocytosis Type 5", "Carrier screening for reproductive planning", "Screening presymptomatic family members"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D76.1 Clinical summary This genetic test identifies pathogenic variants in the STXBP2 gene associated with Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL5).
TEST-5029 UNC13D Gene Hemophagocytic Lymphohistiocytosis Type 3 Genetic Test This test identifies pathogenic variants in the UNC13D gene associated with familial hemophagocytic lymphohistiocytosis type 3 (FHL3).	Peripheral whole blood, Buccal swab, or FTA card	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 UNC13D gene", "Copy Number Variants (CNVs) in the UNC13D gene"] Parameters [] Preparation ["No fasting required", "No medication adjustments required"] Indications ["Suspected familial hemophagocytic lymphohistiocytosis type 3 (FHL3)", "Family history of FHL3", "Consanguinity", "Need for definitive molecular diagnosis for treatment planning (HSCT)", "Genetic counseling and family screening"] Measurement technique Confirm with laboratory Codes LOINC: 82173-8 ICD-10: D76.1 Clinical summary This test identifies pathogenic variants in the UNC13D gene associated with familial hemophagocytic lymphohistiocytosis type 3 (FHL3).

Category overview

Hemophagocytic Lymphohistiocytosis: overview

Navigating sudden, overwhelming systemic inflammation, a dangerously enlarged spleen, and persistent high fevers in a child or adult demands urgent, highly specific diagnostic intervention. Representing a critical, life-saving diagnostic tool within our Genetics and Immunology services, testing for Hemophagocytic Lymphohistiocytosis (HLH) evaluates your DNA for inherited mutations that cause the immune system to violently overreact and damage healthy tissues. Utilizing cutting-edge sequencing technology, this vital molecular screening helps confirm familial HLH, providing the definitive data necessary to safely guide immediate, aggressive immunosuppressive therapies, targeted biological treatments, and critical bone marrow transplant planning. Highly regarded for sensitive, rapid diagnostics among premier diagnostic labs in Dubai and the UAE, DNA Labs guarantees strict patient confidentiality, uncompromising analytical precision, and remarkably fast reporting. Protect your immunological stability—schedule your HLH testing in UAE, arrange a secure clinical sample transfer, or consult our dedicated immunology genetics experts today.

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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.