Monogenic Disorders tests in Dubai & UAE

Compare available Monogenic Disorders 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

2,800.00 AED

Clinical preparation

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Monogenic Disorders test prices

Showing 1–4 of 4 matching tests.

Monogenic Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6237 GCK Gene Hyperinsulinemic Hypoglycemia Type 3 Genetic Test This genetic test identifies pathogenic variants in the GCK gene associated with hyperinsulinemic hypoglycemia type 3.	Whole Blood (EDTA tube), Extracted DNA, or FTA Card Blood Spot	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 GCK gene", "Single nucleotide variants", "Insertions", "Deletions", "Copy number variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Continue prescribed medications unless advised otherwise by a doctor", "Provide Emirates ID and prior genetic reports if available"] Indications ["Suspected hyperinsulinemic hypoglycemia type 3", "Family history of hyperinsulinemic hypoglycemia", "Need for precise genetic diagnosis to guide management", "Cascade screening of family members"] Measurement technique Confirm with laboratory Codes LOINC: 82007-5 ICD-10: E16.1 Clinical summary This genetic test identifies pathogenic variants in the GCK gene associated with hyperinsulinemic hypoglycemia type 3.
TEST-3843 ICK Gene Endocrine-Cerebroosteodysplasia Genetic Test This test identifies pathogenic variants in the ICK gene associated with Endocrine-Cerebroosteodysplasia, a rare multi-system disorder.	Whole Blood, Extracted DNA, or FTA Blood Spot 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 ICK gene", "Single nucleotide variants", "Insertions/deletions", "Copy number variations"] Parameters [] Preparation ["Informed consent must be obtained after thorough pre-test counselling"] Indications ["Suspected Endocrine-Cerebroosteodysplasia", "Evaluation of multi-system disorders with endocrine, neurological, and skeletal features"] Measurement technique Confirm with laboratory Codes LOINC: 47365-9 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants in the ICK gene associated with Endocrine-Cerebroosteodysplasia, a rare multi-system disorder.
TEST-4589 LMNA Gene Restrictive Dermopathy, Lethal Genetic Test This test identifies mutations in the LMNA gene associated with lethal restrictive dermopathy.	Whole blood (EDTA), extracted DNA, or FTA card (dried blood spot)	3-4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LMNA gene mutations", "Nucleotide-level variations"] Parameters [] Preparation [] Indications ["Neonatal diagnosis of lethal restrictive dermopathy", "Carrier detection", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 94246-0 ICD-10: Q82.8, Z15.89, Z14.8 Clinical summary This test identifies mutations in the LMNA gene associated with lethal restrictive dermopathy.
TEST-6052 MLYCD Gene Malonyl‑CoA Decarboxylase Deficiency Genetic Test This genetic test identifies pathogenic variants in the MLYCD gene, confirming a diagnosis of malonyl-CoA decarboxylase deficiency.	Whole blood, extracted DNA, or FTA card specimen	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 MLYCD gene", "Single nucleotide variants", "Small insertions or deletions", "Copy number variations"] Parameters [] Preparation ["No fasting required", "Do not discontinue prescribed carnitine, riboflavin, or anticonvulsant therapies without consultation"] Indications ["Suspected malonyl-CoA decarboxylase deficiency", "Unexplained metabolic crises", "Hypoglycemia", "Cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 93134-2 ICD-10: E71.1 Clinical summary This genetic test identifies pathogenic variants in the MLYCD gene, confirming a diagnosis of malonyl-CoA decarboxylase deficiency.

Category overview

Monogenic Disorders: overview

A family history of a specific, inherited trait or chronic illness warrants proactive molecular insights to protect your future health and secure reproductive confidence. Within our elite Genetics department, testing for Monogenic Disorders evaluates your DNA for single-gene mutations (Mendelian disorders) linked to conditions like cystic fibrosis, sickle cell anemia, or Huntington's disease. By leveraging state-of-the-art sequencing technology, this highly targeted molecular screening confirms your genetic status, providing the definitive clarity needed to assess carrier risks, safely guide proactive medical management, and inform proactive family planning decisions. Trusted for compassionate diagnostic excellence across the best diagnostic labs in the UAE, DNA Labs guarantees strict patient confidentiality, unparalleled diagnostic accuracy, and remarkably fast turnaround times. Safeguard your family’s future—schedule your monogenic disorders testing in UAE, coordinate a comfortable clinic or home sample collection, or reach out to our specialized genetic counselors.

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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.