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.

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480.00–5,200.00 AED

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Cytogenetics test prices

Showing 61–75 of 80 matching tests.

Cytogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1227 High‑Resolution Peripheral Blood Karyotyping (Single) Test This test evaluates the number and structure of chromosomes in peripheral blood cells at a high resolution.	Peripheral Blood, Sodium Heparin	10–12 working days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal number", "Chromosomal structure"] Parameters [] Preparation [] Indications ["Investigation of infertility", "Evaluation of recurrent pregnancy loss", "Diagnosis of haematological malignancies", "Assessment of congenital anomalies", "Detection of chromosomal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 10580-0 ICD-10: Z01.8 Clinical summary This test evaluates the number and structure of chromosomes in peripheral blood cells at a high resolution.
TEST-1144 IGH Gene Break Apart (14q32.3) FISH Test This test detects rearrangements within the IGH gene located on chromosome 14q32.3 using Fluorescence In-Situ Hybridization (FISH). It is used for the diagnosis and prognosis of B-...	Peripheral Blood (Green-top Sodium Heparin Tube) or Bone Marrow Aspirate	4 working days	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IGH gene rearrangements", "Translocations involving 14q32.3"] Parameters [] Preparation ["No fasting required for blood collection", "Completed Chromosome & FISH Requisition Form 17 is mandatory"] Indications ["Diagnosis of B-cell leukemias and lymphomas", "Prognosis and risk stratification in hematologic malignancies", "Guiding targeted therapy"] Measurement technique Confirm with laboratory Codes LOINC: 60528-5 ICD-10: C91.9, C92.9, C90.0 Clinical summary This test detects rearrangements within the IGH gene located on chromosome 14q32.3 using Fluorescence In-Situ Hybridization (FISH). It is used for the diagnosis and prognosis of B-cell leukemias and lymphomas.
TEST-1465 IRF4/MUM1 (IRFA‑MUM1) FISH Test This diagnostic test evaluates for rearrangements in the IRF4 gene using Fluorescence In-Situ Hybridization (FISH). It is crucial for diagnosing and monitoring specific haematologi...	Archival Solid Tissue (FFPE Block or Slides)	7–8 business days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IRF4 gene rearrangement", "Fluorescence In-Situ Hybridization (FISH) signal patterns"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Bring valid DHA-doctor’s prescription", "Bring formalin-fixed paraffin-embedded tissue block or slides"] Indications ["Diagnosis of plasma cell myeloma", "Diagnosis of specific large B-cell lymphomas", "Prognosis assessment", "Minimal residual disease monitoring"] Measurement technique Confirm with laboratory Codes LOINC: 88213-0 ICD-10: C90.00 Clinical summary This diagnostic test evaluates for rearrangements in the IRF4 gene using Fluorescence In-Situ Hybridization (FISH). It is crucial for diagnosing and monitoring specific haematological malignancies.
TEST-1408 MAF/IGH FISH Test (Multiple Myeloma Translocation) This diagnostic test evaluates for the presence of the t(14;16) translocation, a specific genetic rearrangement linked to high-risk multiple myeloma.	Bone Marrow Aspirate (Primary) / Peripheral Blood (Alternative)	3–4 business days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["t(14;16) translocation", "IGH/MAF gene fusion"] Parameters [] Preparation [] Indications ["Diagnosis of multiple myeloma", "Risk stratification in plasma cell disorders", "Treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 49498-9 ICD-10: C90.0 Clinical summary This diagnostic test evaluates for the presence of the t(14;16) translocation, a specific genetic rearrangement linked to high-risk multiple myeloma.
TEST-1398 MDS FISH Panel (del(5q), del(7q), del(20q)) Test This diagnostic test evaluates for the presence of specific chromosomal deletions (del(5q), del(7q), del(20q)) in bone marrow or peripheral blood cells, aiding in the diagnosis and...	Bone Marrow (preferred) or Peripheral Blood	5-7 Days	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Presence of del(5q)", "Presence of del(7q)", "Presence of del(20q)"] Parameters [] Preparation ["No fasting required", "Bring doctor's prescription", "Bring list of current medications"] Indications ["Diagnosis of Myelodysplastic Syndromes (MDS)", "Risk stratification in MDS", "Therapeutic monitoring in MDS", "Guiding treatment decisions (e.g., 5-azacytidine eligibility)"] Measurement technique Confirm with laboratory Codes LOINC: 86903-2 ICD-10: D46.20 Clinical summary This diagnostic test evaluates for the presence of specific chromosomal deletions (del(5q), del(7q), del(20q)) in bone marrow or peripheral blood cells, aiding in the diagnosis and risk stratification of myelodysplastic syndromes.
TEST-1332 Multiple Myeloma FISH Panel (del(11q), del(13q), IgH, del(17p)) Test This diagnostic test evaluates for four specific chromosomal aberrations commonly found in multiple myeloma using FISH technology.	Bone marrow aspirate (primary); peripheral blood (alternative)	5–7 business days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletion of 11q", "Deletion of 13q", "Immunoglobulin heavy chain (IgH) rearrangements", "Deletion of 17p"] Parameters [] Preparation ["No fasting or special preparation is needed.", "A valid physician referral is mandatory.", "Do not alter or discontinue prescribed medications without consulting your physician."] Indications ["Diagnosis of multiple myeloma", "Prognosis assessment in multiple myeloma", "Guidance for treatment selection in multiple myeloma", "Monitoring disease progression"] Measurement technique Confirm with laboratory Codes LOINC: 53756-8 ICD-10: C90.0 Clinical summary This diagnostic test evaluates for four specific chromosomal aberrations commonly found in multiple myeloma using FISH technology.
TEST-1195 MYCN Amplification (FISH) Test This diagnostic test evaluates the presence and degree of MYCN gene amplification in tumor tissue using Fluorescence In-Situ Hybridization (FISH).	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block	4 working days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYCN gene copy number", "Gene amplification status"] Parameters [] Preparation ["No patient preparation is needed"] Indications ["Risk stratification in neuroblastoma", "Guiding therapy decisions in neuroblastoma"] Measurement technique Confirm with laboratory Codes LOINC: 41644-0 ICD-10: C74.9 Clinical summary This diagnostic test evaluates the presence and degree of MYCN gene amplification in tumor tissue using Fluorescence In-Situ Hybridization (FISH).
TEST-1200 NTRK1 Gene Rearrangement Assay (FISH) Test This diagnostic test evaluates for specific genomic rearrangements of the NTRK1 gene in solid tumor tissue.	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block or Slides (Archival Tissue Specimen)	4 working days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NTRK1 gene rearrangements", "Presence of specific fusions"] Parameters [] Preparation ["No special preparation required", "Ensure Genomics Clinical Information Requisition Form (Form 20) is completed"] Indications ["Solid tumors", "Eligibility assessment for TRK inhibitor therapy"] Measurement technique Confirm with laboratory Codes LOINC: 92896-2 ICD-10: Z15.09 Clinical summary This diagnostic test evaluates for specific genomic rearrangements of the NTRK1 gene in solid tumor tissue.
TEST-1207 NTRK3 Gene Rearrangement FISH Assay Test This diagnostic test evaluates for the presence of NTRK3 gene rearrangements (fusions) within solid tumor tissue samples.	Archival Tissue Specimen (FFPE block or slides)	4 Working Days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NTRK3 gene fusions", "Presence of specific genetic alterations"] Parameters [] Preparation ["Submit FFPE tissue block or slides", "Ensure Genomics Clinical Information Requisition Form (Form 20) is completed"] Indications ["Identification of NTRK3 gene fusions in solid tumors", "Guiding targeted therapy with TRK inhibitors", "Diagnosis of NTRK fusion-positive cancers"] Measurement technique Confirm with laboratory Codes LOINC: 92831-1 ICD-10: C49.9 Clinical summary This diagnostic test evaluates for the presence of NTRK3 gene rearrangements (fusions) within solid tumor tissue samples.
TEST-1226 PML/RARA Fusion Gene FISH Test (t(15;17)) This diagnostic test evaluates for the presence of the PML/RARA fusion gene, the defining molecular hallmark of Acute Promyelocytic Leukemia (APL).	Peripheral Whole Blood or Bone Marrow Aspirate	4 working days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PML/RARA fusion gene", "t(15;17) translocation"] Parameters [] Preparation [] Indications ["Suspected Acute Promyelocytic Leukemia (APL)", "Rapid genetic confirmation of t(15;17) translocation"] Measurement technique Confirm with laboratory Codes LOINC: 60511-1 ICD-10: C92.4 Clinical summary This diagnostic test evaluates for the presence of the PML/RARA fusion gene, the defining molecular hallmark of Acute Promyelocytic Leukemia (APL).
TEST-1203 Prader-Willi Syndrome (FISH) Genetic Testing Test This test detects the presence or absence of a microdeletion in the 15q11-q13 region of chromosome 15, the most common cause of Prader-Willi syndrome.	Peripheral Blood (EDTA), Amniotic Fluid, Chorionic Villi, Cord Blood	3-4 business days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 15q11-q13 deletion"] Parameters [] Preparation [] Indications ["Suspected Prader-Willi syndrome", "Neonatal hypotonia", "Feeding difficulties", "Characteristic facial features", "Hyperphagia"] Measurement technique Confirm with laboratory Codes LOINC: 26462-5 ICD-10: Q87.1 Clinical summary This test detects the presence or absence of a microdeletion in the 15q11-q13 region of chromosome 15, the most common cause of Prader-Willi syndrome.
TEST-1208 Prader‑Willi Syndrome FISH Test (SNRPN Locus) This diagnostic test evaluates for the presence of a microdeletion in the SNRPN locus on chromosome 15q11-q13, a key genetic marker for Prader-Willi syndrome.	Whole blood	4 working days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SNRPN locus deletion", "Chromosome 15q11-q13 region"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion (< 2 weeks)"] Indications ["Clinical suspicion of Prader-Willi syndrome", "Evaluation of developmental delay", "Assessment of hypotonia in infancy"] Measurement technique Confirm with laboratory Codes LOINC: 34441-1 ICD-10: Q87.1 Clinical summary This diagnostic test evaluates for the presence of a microdeletion in the SNRPN locus on chromosome 15q11-q13, a key genetic marker for Prader-Willi syndrome.
TEST-2955 Prenatal Diagnosis Panel 1 (Chorionic Villus Biopsy) Test This test evaluates the fetus for multiple inborn errors of metabolism using chorionic villus biopsy.	Chorionic Villus Biopsy (CVS)	5 working days	5,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Enzyme activity", "Metabolite levels", "Genetic mutations"] Parameters [] Preparation ["Requires completed Prenatal Genetic Testing Consent Form (Form 18)", "Prior appointment coordination with logistics team needed"] Indications ["Family history of metabolic disorders", "High-risk pregnancy screening results", "Need for early diagnosis for intervention planning"] Measurement technique Confirm with laboratory Codes LOINC: 82993-6 ICD-10: Z13.228 Clinical summary This test evaluates the fetus for multiple inborn errors of metabolism using chorionic villus biopsy.
TEST-1220 Prenatal FISH Comprehensive Screening Panel 1 Test This diagnostic test evaluates amniotic fluid for specific numerical chromosome abnormalities (trisomies 13, 18, 21, and sex chromosome aneuploidies) using Fluorescence In-Situ Hyb...	Amniotic Fluid	4 Working Days	1,900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Trisomy 13", "Trisomy 18", "Trisomy 21", "Sex chromosome aneuploidies"] Parameters [] Preparation [] Indications ["Prenatal screening for chromosomal anomalies", "Advanced maternal age", "Abnormal ultrasound findings", "Family history of chromosomal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 82151-0 ICD-10: Z36.84 Clinical summary This diagnostic test evaluates amniotic fluid for specific numerical chromosome abnormalities (trisomies 13, 18, 21, and sex chromosome aneuploidies) using Fluorescence In-Situ Hybridization (FISH).
TEST-1216 RET Gene (10q11.2) Rearrangement FISH Test This test detects rearrangements in the RET gene within tissue samples.	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block or Biopsy Slides	4 Working Days	1,700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RET gene rearrangements", "Oncogenic alterations"] Parameters [] Preparation [] Indications ["Confirmed or suspected medullary thyroid carcinoma (MTC)", "Confirmed or suspected papillary thyroid carcinoma (PTC)", "Consideration of RET-targeted therapy", "Risk stratification in hereditary thyroid cancer syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 60521-6 ICD-10: C73 Clinical summary This test detects rearrangements in the RET gene within tissue samples.

Category overview

Cytogenetics: overview

Understanding your genetic blueprint can provide invaluable clarity for both proactive health planning and specialized medical care. The Cytogenetics division at DNA Labs UAE employs cutting-edge chromosomal microarray and FISH technologies to analyze cellular genetics. Whether assessing hereditary conditions or guiding specialized treatments, our advanced cytogenetic testing in the UAE acts as a critical navigational tool for your physician. Ranked among the top diagnostic labs in Dubai/UAE, we handle your sensitive genetic data with absolute confidentiality, ensuring you receive fast, precise, and secure results. Empower your medical decisions. Browse our cytogenetics services below, arrange a private home collection, or speak with our genetics specialists today.

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Cytogenetics tests in Dubai & UAE

Cytogenetics test prices

Cytogenetics: overview

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