Diagnostic options · UAE

Cytogenetics tests in Dubai & UAE

Compare available Cytogenetics 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

550.00–3,600.00 AED

Clinical preparation

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Cytogenetics test prices

Showing 1–15 of 30 matching tests.

Cytogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-115 Acute Lymphoblastic Leukemia (ALL) Cytogenetics Panel Test This diagnostic test evaluates chromosomal abnormalities in leukemia cells using karyotyping and FISH.	Bone marrow aspirate and peripheral blood	4 working days	2,700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal abnormalities (e.g., translocations, aneuploidy)", "Specific genetic markers (e.g., t(9;22), t(12;21))"] Parameters [] Preparation [] Indications ["Diagnosis of ALL", "Risk stratification in ALL", "Guiding therapeutic decisions (e.g., TKI eligibility, HSCT)", "Monitoring response to therapy"] Measurement technique Confirm with laboratory Codes LOINC: 48801-6 ICD-10: C91.00 Clinical summary This diagnostic test evaluates chromosomal abnormalities in leukemia cells using karyotyping and FISH.
TEST-109 Acute Myeloid Leukemia (AML) Cytogenetics Panel Test This test evaluates chromosomal abnormalities in blood and bone marrow cells to diagnose, classify, and determine the prognosis of Acute Myeloid Leukemia (AML).	Peripheral Whole Blood & Bone Marrow	4 working days	3,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal aberrations (translocations, inversions, deletions, additions)", "Karyotype complexity", "Specific AML-defining genetic markers"] Parameters [] Preparation ["No fasting required.", "Inform physician about all anticoagulants.", "Complete Chromosome and FISH Analysis Requisition Form (Form 17)."] Indications ["Diagnosis of suspected Acute Myeloid Leukemia (AML)", "Risk stratification and prognostication in confirmed AML", "Guiding therapeutic decisions in AML", "Monitoring for minimal residual disease (in specific contexts)"] Measurement technique Confirm with laboratory Codes LOINC: 91836-7 ICD-10: C92.0 Clinical summary This test evaluates chromosomal abnormalities in blood and bone marrow cells to diagnose, classify, and determine the prognosis of Acute Myeloid Leukemia (AML).
TEST-1852 AML Cytogenetics & FISH Panel Test This test evaluates chromosomal abnormalities and gene rearrangements associated with acute myeloid leukemia (AML). It combines karyotyping and Fluorescence In Situ Hybridization (...	Bone marrow aspirate or peripheral blood	10 days (FISH results available within 3–5 days for critical markers)	2,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal rearrangements (karyotyping)", "Specific gene rearrangements (FISH: AML/ETO, inv(16), PML/RARA, MLL)"] Parameters [] Preparation ["No special preparation required", "Doctor’s prescription and clinical history form are mandatory"] Indications ["Diagnosis of acute myeloid leukemia (AML)", "Risk stratification in AML", "Guiding targeted therapy selection in AML"] Measurement technique Confirm with laboratory Codes LOINC: 79521-9 ICD-10: C92.00, C92.01, C92.02 Clinical summary This test evaluates chromosomal abnormalities and gene rearrangements associated with acute myeloid leukemia (AML). It combines karyotyping and Fluorescence In Situ Hybridization (FISH) to identify specific genetic markers.
TEST-1858 AML FISH Panel Test This diagnostic test evaluates for the presence of four specific chromosomal rearrangements commonly found in Acute Myeloid Leukemia (AML) using Fluorescence In-Situ Hybridization...	Bone Marrow Aspirate or Peripheral Blood	10 Business Days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["t(8;21)(q22;q22) / AML1-ETO rearrangement", "inv(16)(p13.1q22) / CBFB-MYH11 rearrangement", "t(15;17)(q24.1;q21.2) / PML-RARA rearrangement", "Rearrangements involving 11q23 / MLL (KMT2A)"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}] Preparation ["No fasting required", "Inform doctor about anticoagulant medications", "Valid physician prescription required"] Indications ["Diagnosis of Acute Myeloid Leukemia (AML)", "Risk stratification in AML", "Guidance for targeted therapy selection in AML"] Measurement technique Confirm with laboratory Codes LOINC: 96589-0 ICD-10: C92.00, C92.50, Z15.01 Clinical summary This diagnostic test evaluates for the presence of four specific chromosomal rearrangements commonly found in Acute Myeloid Leukemia (AML) using Fluorescence In-Situ Hybridization (FISH). It provides rapid genetic information essential for AML classification and treatment planning.
TEST-1841 BCL2 Gene Rearrangement, FISH Test This test detects rearrangements in the BCL2 gene, commonly associated with follicular lymphoma and other B-cell malignancies.	Bone Marrow / Peripheral Blood	3–4 business days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCL2 gene rearrangement", "t(14;18) translocation"] Parameters [] Preparation ["No fasting required", "Inform phlebotomist about medications or bleeding conditions", "Arrange for a companion if bone marrow aspiration is performed"] Indications ["Suspected lymphoma", "Diagnosis of follicular lymphoma", "Risk stratification", "Monitoring minimal residual disease"] Measurement technique Confirm with laboratory Codes LOINC: 48532-1 ICD-10: C82.9 Clinical summary This test detects rearrangements in the BCL2 gene, commonly associated with follicular lymphoma and other B-cell malignancies.
TEST-1835 BCL2/IGH (t14;18) Translocation FISH Test This diagnostic test evaluates for the presence of the BCL2/IGH (t14;18) chromosomal translocation in tumor tissue using FISH.	Archival Tissue Specimen (FFPE tissue blocks or slides)	7–8 working days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCL2/IGH (t14;18) chromosomal translocation", "Gene rearrangement"] Parameters [] Preparation ["No fasting required", "No specific medication adjustments needed unless advised by physician"] Indications ["Suspected diagnosis of follicular lymphoma", "Monitoring for minimal residual disease", "Therapeutic stratification"] Measurement technique Confirm with laboratory Codes LOINC: 87783-7 ICD-10: C82.9 Clinical summary This diagnostic test evaluates for the presence of the BCL2/IGH (t14;18) chromosomal translocation in tumor tissue using FISH.
TEST-1754 Bone Marrow Karyotyping Analysis Test This test analyzes the chromosomes within bone marrow cells to detect abnormalities associated with blood cancers and genetic disorders.	Bone marrow aspirate	7–8 days	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal number", "Chromosomal structure"] Parameters [] Preparation ["Stop blood thinners 5 days prior after consulting your physician", "Fast for 6 hours", "Arrange for someone to drive you home post-procedure", "A valid DHA-licensed physician’s prescription is mandatory"] Indications ["Diagnosis of leukemia (AML, CML, ALL)", "Diagnosis of myelodysplastic syndromes (MDS)", "Diagnosis of myeloproliferative neoplasms (MPN)", "Workup for recurrent pregnancy loss", "Investigation of constitutional genetic syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 623-7 ICD-10: Z01.89 Clinical summary This test analyzes the chromosomes within bone marrow cells to detect abnormalities associated with blood cancers and genetic disorders.
TEST-1358 Chromosomal Microarray 60K with Karyotyping Test This diagnostic test evaluates chromosomal structure and copy number variations to identify genetic abnormalities.	Peripheral Blood, Cord Blood, Fetal Blood (sodium-heparin bottle)	7–9 working days	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Chromosomal Aneuploidy", "Balanced Structural Rearrangements"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab of any anticoagulant therapy."] Indications ["Paediatric developmental delay", "Prenatal diagnosis", "Recurrent pregnancy loss", "Haematological malignancy screening", "Unexplained intellectual disability", "Autism spectrum disorder investigation"] Measurement technique Confirm with laboratory Codes LOINC: 82119-6 ICD-10: Z01.818 Clinical summary This diagnostic test evaluates chromosomal structure and copy number variations to identify genetic abnormalities.
TEST-1653 Chromosome 13q Deletion (Del(13q)) Analysis Test This diagnostic test evaluates for the presence of a deletion in the long arm of chromosome 13 (13q) using Fluorescence In-Situ Hybridization (FISH).	Bone marrow (preferred) or peripheral blood	3–4 days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Loss of the long arm of chromosome 13 (13q)", "Presence of del(13q) in plasma cells or B-lymphocytes"] Parameters [{"name": "Chromosome 13q Deletion Status", "reference_range": "Negative (No deletion detected)"}] Preparation ["Doctor’s prescription is mandatory.", "Specific fasting instructions may be provided during scheduling if sedation is planned."] Indications ["Risk stratification in Multiple Myeloma (MM)", "Risk stratification in Chronic Lymphocytic Leukemia (CLL)", "Guidance for therapy selection in MM/CLL"] Measurement technique Confirm with laboratory Codes LOINC: 61853-0 ICD-10: C90.0, C91.1 Clinical summary This diagnostic test evaluates for the presence of a deletion in the long arm of chromosome 13 (13q) using Fluorescence In-Situ Hybridization (FISH).
TEST-1730 Chromosome 21 FISH Test This diagnostic test rapidly evaluates the number of chromosome 21 copies in cells.	Amniotic Fluid, Chorionic Villi, Cord Blood, Bone Marrow	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 21 copy number", "Trisomy 21 presence"] Parameters [] Preparation [] Indications ["Prenatal screening for Down syndrome", "Monitoring hyperdiploidy in oncology"] Measurement technique Confirm with laboratory Codes LOINC: 21198-3 ICD-10: Q90.9 Clinical summary This diagnostic test rapidly evaluates the number of chromosome 21 copies in cells.
TEST-615 Chromosome Analysis (Karyotype) Blood Test This diagnostic test evaluates the number and structure of an individual's chromosomes to identify abnormalities.	Peripheral Whole Blood (Sodium Heparin Tube)	10–12 working days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome number", "Chromosome structure"] Parameters [] Preparation ["No fasting required", "Completed requisition form from referring physician is mandatory", "Written consent from legal guardian for minors"] Indications ["Diagnosis of genetic syndromes", "Evaluation of recurrent pregnancy loss", "Investigation of intellectual disability", "Diagnosis of hematologic malignancies", "Assessment of infertility"] Measurement technique Confirm with laboratory Codes LOINC: 55231-0 ICD-10: Z01.8 Clinical summary This diagnostic test evaluates the number and structure of an individual's chromosomes to identify abnormalities.
TEST-638 Chromosome Analysis Cord Blood Test This diagnostic test evaluates the fetal chromosomes for numerical and structural abnormalities.	Cord blood	10 working days	600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Fetal Chromosomes", "Numerical Abnormalities (e.g., Trisomies)", "Structural Abnormalities (e.g., Deletions, Translocations)"] Parameters [] Preparation ["No fasting required", "Complete mandatory consent and requisition forms", "Provide accurate gestational age"] Indications ["High-risk pregnancy", "Abnormal screening test results", "Advanced maternal age", "Family history of chromosomal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 49095-5 ICD-10: Z36.0, O35.1, Q99.9 Clinical summary This diagnostic test evaluates the fetal chromosomes for numerical and structural abnormalities.
TEST-617 Chromosome Analysis for Hematologic Malignancy (Cytogenetic Karyotyping) Test This diagnostic test evaluates chromosomal structure and number in blood or bone marrow cells to detect abnormalities associated with hematologic malignancies.	Bone Marrow or Peripheral Blood	4 working days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Numerical chromosomal abnormalities (aneuploidy)", "Structural chromosomal abnormalities (translocations, deletions, inversions)"] Parameters [] Preparation ["No fasting required", "Inform staff about blood thinners or bleeding disorders", "Complete the mandatory Chromosome & FISH Analysis Requisition Form (Form 17)"] Indications ["Diagnosis of leukemia (e.g., AML, ALL, CML, CLL)", "Diagnosis of myelodysplastic syndromes (MDS)", "Risk stratification in hematologic malignancies", "Monitoring response to therapy", "Detection of minimal residual disease (MRD)"] Measurement technique Confirm with laboratory Codes LOINC: 33717-0 ICD-10: C91.90, D46.9 Clinical summary This diagnostic test evaluates chromosomal structure and number in blood or bone marrow cells to detect abnormalities associated with hematologic malignancies.
TEST-637 Chromosome Interphase Profiling for Products of Conception (POC) Test This diagnostic test evaluates products of conception (POC) for common numerical chromosomal abnormalities (aneuploidies) using Fluorescence In-Situ Hybridization (FISH). It identi...	Placental or Fetal Tissue (Products of Conception)	7 Working Days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Numerical chromosomal abnormalities (aneuploidies)", "Presence of specific aneuploidies (chromosomes 13, 18, 21, X, Y)"] Parameters [] Preparation ["No dietary fasting required", "No medication adjustment required"] Indications ["Investigation of recurrent pregnancy loss", "Evaluation of fetal tissue after miscarriage", "Assessment of chromosomal abnormalities in products of conception"] Measurement technique Confirm with laboratory Codes LOINC: 53760-6 ICD-10: O02.1, O36.4, N96 Clinical summary This diagnostic test evaluates products of conception (POC) for common numerical chromosomal abnormalities (aneuploidies) using Fluorescence In-Situ Hybridization (FISH). It identifies aneuploidies of chromosomes 13, 18, 21, X, and Y.
TEST-1726 Chromosomes 13 & 21 (FISH) Test This diagnostic test evaluates the number of copies of chromosomes 13 and 21 in fetal cells obtained from amniotic fluid, chorionic villi, or cord blood.	Amniotic Fluid, Chorionic Villi, Cord Blood	3–4 Business Days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy number variation of chromosome 13", "Copy number variation of chromosome 21"] Parameters [] Preparation [] Indications ["Prenatal screening for Down syndrome (trisomy 21)", "Prenatal screening for Patau syndrome (trisomy 13)", "Monitoring acquired trisomies in certain hematological disorders"] Measurement technique Confirm with laboratory Codes LOINC: ['19808-0', '19809-8'] ICD-10: ['Q90.9', 'Q91.7'] Clinical summary This diagnostic test evaluates the number of copies of chromosomes 13 and 21 in fetal cells obtained from amniotic fluid, chorionic villi, or cord blood.

Category overview

Cytogenetics: overview

Achieving a comprehensive understanding of your foundational chromosomal architecture is essential when navigating complex reproductive challenges, developmental delays, or suspected oncological conditions. As the cornerstone of our advanced Genetics services, comprehensive Cytogenetics screening involves the high-resolution microscopic and molecular evaluation of your cells to detect significant structural abnormalities, deletions, or duplications. By leveraging cutting-edge diagnostic technology, this expansive foundational profiling delivers the definitive data needed to diagnose complex genetic disorders and blood cancers, safely guiding your healthcare provider’s highly customized therapeutic strategies, targeted oncology protocols, and proactive family planning. Trusted for cytogenetic excellence among premier diagnostic labs in Dubai and the UAE, DNA Labs is steadfastly committed to strict patient confidentiality, uncompromising analytical accuracy, and incredibly efficient turnaround times. Prioritize your specialized healthcare journey—book your cytogenetics testing in UAE, arrange a seamless clinical sample collection, or consult our expert medical professionals today.

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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.