Fanconi Anemia tests in Dubai & UAE

Compare available Fanconi Anemia 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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Fanconi Anemia test prices

Showing 1–8 of 8 matching tests.

Fanconi Anemia diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5079 ERCC4 (FANCQ) Gene Genetic Test for Fanconi Anemia This genetic test identifies pathogenic variants in the ERCC4 (FANCQ) gene associated with Fanconi anemia complementation group Q.	Peripheral whole blood or FTA card spot	3 to 4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in ERCC4 gene coding exons and splice junctions"] Parameters [] Preparation ["None specified"] Indications ["Suspected Fanconi anemia", "Family history of Fanconi anemia", "Genetic counseling for reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 21634-2 ICD-10: D61.09 Clinical summary This genetic test identifies pathogenic variants in the ERCC4 (FANCQ) gene associated with Fanconi anemia complementation group Q.
TEST-6265 FANCA Gene Fanconi Anemia Type A Genetic Test This test identifies pathogenic variants in the FANCA gene associated with Fanconi Anemia Type A.	3–5 mL whole blood (EDTA tube), dried blood spot (FTA card), or previously extracted DNA	21–28 business days (~3–4 weeks)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in FANCA gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Diagnosis of suspected Fanconi anemia type A", "Carrier screening in at-risk family members", "Presymptomatic testing in at-risk family members", "Variant of Uncertain Significance (VUS) resolution"] Measurement technique Confirm with laboratory Codes LOINC: 21661-0 ICD-10: D61.09 Clinical summary This test identifies pathogenic variants in the FANCA gene associated with Fanconi Anemia Type A.
TEST-6364 FANCB Gene Fanconi Anemia Type B Genetic Test This test detects pathogenic variants in the FANCB gene, which are associated with Fanconi anemia type B, an X-linked inherited bone marrow failure disorder.	Whole blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card)	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 FANCB gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number alterations"] Parameters [] Preparation ["No fasting required", "Recommend being well-hydrated prior to home phlebotomy", "Submit detailed clinical history including prior transfusion dates, medication lists, and corticosteroid or androgen therapy"] Indications ["Patients presenting with congenital anomalies", "Patients with hematological cytopenias", "Patients with a family history suggestive of Fanconi anemia", "Carrier testing in at-risk female relatives", "Preimplantation genetic diagnosis planning"] Measurement technique Confirm with laboratory Codes LOINC: 101402-7 ICD-10: D61.09, Z13.79, Z15.09 Clinical summary This test detects pathogenic variants in the FANCB gene, which are associated with Fanconi anemia type B, an X-linked inherited bone marrow failure disorder.
TEST-6366 FANCE Gene (Fanconi Anemia Type E) Genetic Test This genetic test evaluates the FANCE gene for mutations associated with Fanconi Anemia type E.	Peripheral Whole Blood / Extracted DNA / FTA Card	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 FANCE gene", "Copy Number Variations (CNV) in the FANCE gene"] Parameters [] Preparation ["No fasting or dietary changes required", "Continue prescribed medications", "Attend pre-test genetic counseling session"] Indications ["Suspected Fanconi Anemia type E", "Family history of Fanconi Anemia", "Carrier screening", "Cancer predisposition assessment"] Measurement technique Confirm with laboratory Codes LOINC: 93213-9 ICD-10: D61.06 Clinical summary This genetic test evaluates the FANCE gene for mutations associated with Fanconi Anemia type E.
TEST-6369 FANCG Gene Fanconi Anemia Type G Genetic Test This test identifies pathogenic variants in the FANCG gene associated with Fanconi anemia type G.	Whole Blood (EDTA), Extracted DNA, or One Drop of Blood on FTA Card	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 FANCG gene", "Molecular diagnosis of Fanconi anemia type G"] Parameters [] Preparation ["No fasting or special preparation is required"] Indications ["Confirm Fanconi anemia type G", "Evaluate hereditary cancer predisposition", "Diagnostic workup for specific congenital anomalies"] Measurement technique Confirm with laboratory Codes LOINC: 83078-3 ICD-10: D61.09, Z15.0, Z31.440 Clinical summary This test identifies pathogenic variants in the FANCG gene associated with Fanconi anemia type G.
TEST-6280 FANCI Gene Fanconi Anemia Type I Genetic Test This test identifies pathogenic variants in the FANCI gene associated with Fanconi anemia type I.	Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card)	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 FANCI gene", "Single nucleotide variants", "Small indels", "Copy number variants"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your treating physician"] Indications ["Diagnosis of Fanconi anemia type I", "Carrier screening", "Family planning", "Guiding haematopoietic stem cell transplant decisions"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: D61.09 Clinical summary This test identifies pathogenic variants in the FANCI gene associated with Fanconi anemia type I.
TEST-6284 FANCL Gene Fanconi Anemia Type L Genetic Test This test evaluates the FANCL gene for pathogenic variants associated with Fanconi anemia type L, a rare inherited bone marrow failure syndrome.	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 FANCL gene", "Coding exons and splice sites of the FANCL gene"] Parameters [] Preparation [] Indications ["Individuals with a family history of Fanconi anemia", "Individuals with unexplained bone marrow failure", "Individuals with early-onset cancers", "Individuals recommended for testing by a genetic counsellor"] Measurement technique Confirm with laboratory Codes LOINC: 100152-5 ICD-10: D61.0, Z15.0, Z31.430 Clinical summary This test evaluates the FANCL gene for pathogenic variants associated with Fanconi anemia type L, a rare inherited bone marrow failure syndrome.
TEST-6373 FANCM Gene Fanconi Anemia Type M Genetic Test This genetic test evaluates the FANCM gene for mutations associated with Fanconi anemia type M, a disorder causing bone marrow failure and cancer predisposition.	Peripheral whole blood (venous or FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FANCM gene sequence", "FANCM gene copy number variations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without physician advice"] Indications ["Suspected Fanconi anemia type M", "Family history of Fanconi anemia", "Pre-implantation genetic diagnosis (PGD) carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: D61.09 Clinical summary This genetic test evaluates the FANCM gene for mutations associated with Fanconi anemia type M, a disorder causing bone marrow failure and cancer predisposition.

Category overview

Fanconi Anemia: overview

Dealing with unexplained severe bone marrow failure, unusual physical abnormalities, or an extreme predisposition to early cancers requires incredibly precise, urgent diagnostic clarity. As a rare disease specialty within our advanced Genetics services, Fanconi Anemia testing evaluates your cells for a unique inability to repair damaged DNA, leading to catastrophic cellular breakdowns. Utilizing state-of-the-art molecular and cytogenetic technology, this vital screening helps confirm this complex inherited disorder, providing the definitive data necessary to safely guide critical, specialized pediatric hematology care, tailored bone marrow transplant planning, and rigorous preventative oncology monitoring. Trusted for sensitive pediatric and oncological diagnostics across premier diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, uncompromising diagnostic accuracy, and rapid, dependable turnaround times. Support your foundational cellular health—schedule your Fanconi anemia testing in UAE, coordinate a secure clinical sample transfer, or consult our dedicated medical genetics professionals 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.