Genetic Panel tests in Dubai & UAE

Compare available Genetic Panel 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

3,000.00–4,800.00 AED

Clinical preparation

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Genetic Panel test prices

Showing 1–7 of 7 matching tests.

Genetic Panel diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1842 Arthrogryposis and Congenital Myasthenic Syndrome Gene Panel Test This test evaluates for pathogenic genetic variants associated with Arthrogryposis Multiplex Congenita and Congenital Myasthenic Syndromes.	Amniotic fluid, Chorionic villi, or Peripheral blood	4–6 weeks	4,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in genes associated with Arthrogryposis Multiplex Congenita", "Pathogenic variants in genes associated with Congenital Myasthenic Syndromes"] Parameters [] Preparation ["No specific fasting required", "Inform physician about all current medications"] Indications ["Suspected diagnosis of Arthrogryposis Multiplex Congenita", "Suspected diagnosis of Congenital Myasthenic Syndrome", "Family history of related genetic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 90280-9 ICD-10: Q74.3, G70.2 Clinical summary This test evaluates for pathogenic genetic variants associated with Arthrogryposis Multiplex Congenita and Congenital Myasthenic Syndromes.
TEST-3948 Atypical Hemolytic Uremic Syndrome (aHUS) Panel Genetic Test This test identifies pathogenic variants in over 20 genes associated with atypical hemolytic uremic syndrome (aHUS) using next-generation sequencing.	Peripheral whole blood (EDTA tube) or FTA card	3–4 weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in complement regulatory genes", "Pathogenic variants in coagulation factor genes"] Parameters [] Preparation ["No fasting required", "Inform lab of recent blood transfusions (within 1 week)", "Inform lab of current medications"] Indications ["Suspected diagnosis of atypical hemolytic uremic syndrome (aHUS)", "Family history of aHUS", "Guiding targeted therapy selection (Eculizumab, Ravulizumab)", "Family cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 93505-2 ICD-10: D59.3 Clinical summary This test identifies pathogenic variants in over 20 genes associated with atypical hemolytic uremic syndrome (aHUS) using next-generation sequencing.
TEST-3945 Congenital Adrenal Hyperplasia Panel Genetic Test This test evaluates for genetic mutations associated with Congenital Adrenal Hyperplasia (CAH). It provides a definitive molecular diagnosis for this endocrine disorder.	Peripheral Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card)	3–4 Weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in CYP21A2 gene", "Mutations in other relevant CAH genes"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed unless advised by physician"] Indications ["Suspected CAH", "Family history of CAH", "Ambiguous genitalia in newborns"] Measurement technique Confirm with laboratory Codes LOINC: 82124-1 ICD-10: E25.0 Clinical summary This test evaluates for genetic mutations associated with Congenital Adrenal Hyperplasia (CAH). It provides a definitive molecular diagnosis for this endocrine disorder.
TEST-1314 Neuronal Ceroid Lipofuscinosis Gene Panel Test This test identifies pathogenic variants in genes linked to Neuronal Ceroid Lipofuscinosis (NCL), a group of inherited neurodegenerative disorders.	Whole Blood (Peripheral)	4–6 weeks	4,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in NCL-associated genes (CLN1–CLN14, KCTD7, MFSD8, etc.)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Suspected diagnosis of Neuronal Ceroid Lipofuscinosis", "Family history of NCL", "Neurological symptoms suggestive of NCL", "Ophthalmological findings suggestive of NCL"] Measurement technique Confirm with laboratory Codes LOINC: 96623-4 ICD-10: E75.4, Z13.9 Clinical summary This test identifies pathogenic variants in genes linked to Neuronal Ceroid Lipofuscinosis (NCL), a group of inherited neurodegenerative disorders.
TEST-1260 Pancreatic Mutation Panel Test This test evaluates germline mutations in genes associated with hereditary pancreatic cancer susceptibility.	Peripheral Whole Blood	4–6 weeks	3,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Germline mutations", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number alterations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "No specific medication or diet restrictions"] Indications ["Individuals with a personal or family history suggestive of hereditary pancreatic cancer syndrome", "Pre-surgical evaluation for certain cancers", "Assessment of genetic risk for pancreatic cancer"] Measurement technique Confirm with laboratory Codes LOINC: 89768-8 ICD-10: Z15.03 Clinical summary This test evaluates germline mutations in genes associated with hereditary pancreatic cancer susceptibility.
TEST-3701 Spastic Paraplegia Panel (NGS) Genetic Test This test identifies pathogenic variants in genes associated with hereditary spastic paraplegia.	Whole Blood (EDTA tube)	3–4 Weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in >50 HSP genes"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Complete clinical history form", "Provide family pedigree chart if possible"] Indications ["Individuals with suspected hereditary spastic paraplegia", "Family members of individuals diagnosed with HSP"] Measurement technique Confirm with laboratory Codes LOINC: 94485-8 ICD-10: G11.4 Clinical summary This test identifies pathogenic variants in genes associated with hereditary spastic paraplegia.
TEST-1097 Spinal Muscular Atrophy (SMA) Gene Panel Test This test evaluates the SMN1 and SMN2 genes for pathogenic variants associated with Spinal Muscular Atrophy (SMA).	Amniotic Fluid, Chorionic Villi, Peripheral Blood	4–6 weeks	4,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SMN1 gene variants", "SMN2 gene variants", "Copy number variations (deletions/duplications)"] Parameters [] Preparation [] Indications ["Confirmatory diagnosis of SMA", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 92661-8 ICD-10: G12.9 Clinical summary This test evaluates the SMN1 and SMN2 genes for pathogenic variants associated with Spinal Muscular Atrophy (SMA).

Category overview

Genetic Panel: overview

Investigating complex, overlapping clinical symptoms demands a targeted, high-resolution diagnostic approach to ensure no crucial piece of the puzzle is missed. Within our specialized Genetics services, a Genetic Panel focuses on a curated selection of genes simultaneously that are known to cause specific medical conditions, such as hereditary cancers or cardiac disorders. Utilizing cutting-edge sequencing technology, this highly targeted molecular screening delivers the exact clarity needed to uncover precise genetic drivers, safely guiding your healthcare provider’s highly personalized treatment plans and proactive monitoring. Widely respected among the best diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, unparalleled diagnostic accuracy, and remarkably fast turnaround times for sensitive cases. Empower your customized medical care—schedule your genetic panel testing in UAE, coordinate a secure sample transfer, or consult our expert medical genetics team 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.