Rett Syndrome tests in Dubai & UAE

Compare available Rett Syndrome 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

1,400.00–2,800.00 AED

Clinical preparation

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Rett Syndrome test prices

Showing 1–5 of 5 matching tests.

Rett Syndrome diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1395 MECP2 Full Gene Mutation Analysis (Rett Syndrome) Test This test identifies pathogenic variants within the MECP2 gene, the primary cause of Rett syndrome.	Peripheral whole blood	8–10 days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MECP2 gene sequence", "Pathogenic variants in MECP2"] Parameters [] Preparation ["No special fasting required", "No medication adjustment required"] Indications ["Clinical suspicion of Rett syndrome", "Confirmation of Rett syndrome diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21681-0 ICD-10: F84.2 Clinical summary This test identifies pathogenic variants within the MECP2 gene, the primary cause of Rett syndrome.
TEST-2406 MECP2 Gene Rett Syndrome Genetic Test This genetic test analyzes the MECP2 gene to identify pathogenic variants associated with Rett syndrome and related neurodevelopmental disorders.	Peripheral whole blood (5 mL EDTA tube)	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 the MECP2 gene", "Coding exons", "Conserved regulatory regions"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any anticoagulant therapy"] Indications ["Suspected Rett syndrome based on clinical presentation", "Neonatal encephalopathy with MECP2 involvement", "Atypical Rett syndrome presentation"] Measurement technique Confirm with laboratory Codes LOINC: 79973-8 ICD-10: F84.2 Clinical summary This genetic test analyzes the MECP2 gene to identify pathogenic variants associated with Rett syndrome and related neurodevelopmental disorders.
TEST-5647 MECP2 Gene Rett Syndrome Preserved Speech Variant Genetic Test This genetic test identifies pathogenic variants in the MECP2 gene, specifically associated with the preserved speech variant of Rett syndrome.	Blood, Extracted DNA, FTA 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 MECP2 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected Rett syndrome with preserved speech", "Neurodevelopmental disorders", "Differentiation from other genetic conditions"] Measurement technique Confirm with laboratory Codes LOINC: 21634-2 ICD-10: F84.2 Clinical summary This genetic test identifies pathogenic variants in the MECP2 gene, specifically associated with the preserved speech variant of Rett syndrome.
TEST-1161 Rett Syndrome Deletion & Duplication Detection (MLPA) Test This test detects deletions or duplications within the MECP2 gene, which are the primary cause of Rett syndrome.	Peripheral Whole Blood (EDTA tube)	7–10 calendar days	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy number variations (deletions/duplications) in the MECP2 gene"] Parameters [] Preparation ["No specific fasting required", "Avoid sample collection during active febrile illness"] Indications ["Clinical suspicion of Rett syndrome", "Developmental delay or regression in females", "Family history of Rett syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 82897-9 ICD-10: F84.2 Clinical summary This test detects deletions or duplications within the MECP2 gene, which are the primary cause of Rett syndrome.
TEST-3007 Rett Syndrome Detection Test This test detects mutations within the MECP2 gene, the primary cause of Rett Syndrome.	Whole blood	13 days from receipt (sample by 11 AM)	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MECP2 gene variants", "Single-nucleotide variants", "Small insertions/deletions (indels)"] Parameters [{"name": "MECP2 Gene Sequencing", "reference_range": "No pathogenic variants detected"}] Preparation ["No special preparation such as fasting is required", "Ensure child is well-hydrated", "Dress child in comfortable clothing"] Indications ["Suspected Rett Syndrome based on clinical presentation", "Developmental delay or regression", "Family history of Rett Syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 21613-5 ICD-10: F84.2 Clinical summary This test detects mutations within the MECP2 gene, the primary cause of Rett Syndrome.

Category overview

Rett Syndrome: overview

Navigating severe developmental regression or unexplained neurological symptoms in a young child demands immediate, precise diagnostic clarity to ensure they receive the best possible specialized support. Within our highly specialized Genetics department, Rett Syndrome testing meticulously analyzes the MECP2 gene for mutations that disrupt normal brain development. Utilizing state-of-the-art diagnostic technology, this critical molecular screening helps confirm this complex neurodevelopmental disorder, providing the definitive data necessary to safely guide specialized pediatric neurology care and supportive therapeutic strategies. Highly regarded for compassionate pediatric diagnostics among the best diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, unparalleled diagnostic precision, and highly efficient reporting. Find the definitive diagnostic answers you need—book your Rett syndrome testing in UAE, arrange a secure clinical sample collection, or connect with our dedicated 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.