Charcot-Marie-Tooth Disease tests in Dubai & UAE

Compare available Charcot-Marie-Tooth Disease 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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2,800.00 AED

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Charcot-Marie-Tooth Disease test prices

Showing 1–10 of 10 matching tests.

Charcot-Marie-Tooth Disease diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4037 CTDP1 Gene Sequencing for Charcot-Marie-Tooth Disease Type 4 Test This test analyzes the CTDP1 gene to detect pathogenic variants associated with Charcot-Marie-Tooth disease type 4.	Peripheral whole blood (3-5 mL in EDTA)	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CTDP1 gene sequence", "Pathogenic variants in CTDP1"] Parameters [] Preparation [] Indications ["Suspected Charcot-Marie-Tooth disease type 4", "Family history of CMT4", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 60095-4 ICD-10: G60.0, G60.8 Clinical summary This test analyzes the CTDP1 gene to detect pathogenic variants associated with Charcot-Marie-Tooth disease type 4.
TEST-3987 DYNC1H1 Gene Charcot-Marie-Tooth Disease Axonal Type 20 Genetic Test This genetic test evaluates the DYNC1H1 gene for pathogenic variants associated with axonal Charcot-Marie-Tooth disease type 20.	Peripheral Whole Blood (5–10 ml in EDTA tube)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DYNC1H1 gene sequence", "DYNC1H1 gene copy number variations"] Parameters [] Preparation ["No special preparation such as fasting is required.", "Stay well-hydrated before the collection.", "Inform the phlebotomist if you have a history of bleeding disorders or are taking anticoagulant medications."] Indications ["Differential diagnosis of Axonal CMT type 20 (CMT2O)", "Confirmation of suspected CMT2O"] Measurement technique Confirm with laboratory Codes LOINC: 82317-2 ICD-10: G60.0 Clinical summary This genetic test evaluates the DYNC1H1 gene for pathogenic variants associated with axonal Charcot-Marie-Tooth disease type 20.
TEST-4103 FGD4 Gene CMT4H Genetic Test This test identifies pathogenic variants in the FGD4 gene associated with autosomal recessive Charcot-Marie-Tooth disease type 4H (CMT4H).	Peripheral Whole Blood (EDTA)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in FGD4 gene", "Single-nucleotide variants", "Insertions", "Deletions", "Copy-number alterations"] Parameters [] Preparation ["A detailed clinical history is required", "Formal genetic counselling session with pedigree analysis is mandatory"] Indications ["Suspected Charcot-Marie-Tooth disease type 4H", "Inherited neuropathy", "Autosomal recessive inheritance pattern"] Measurement technique Confirm with laboratory Codes LOINC: 21656-9 ICD-10: G60.0 Clinical summary This test identifies pathogenic variants in the FGD4 gene associated with autosomal recessive Charcot-Marie-Tooth disease type 4H (CMT4H).
TEST-4176 GJB1 Gene (Dejerine-Sottas Disease) Next-Generation Sequencing Genetic Test This test evaluates the GJB1 gene for pathogenic variants associated with Dejerine-Sottas disease.	Peripheral whole blood (3-5 mL in EDTA tube)	4 – 5 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GJB1 gene coding region", "Pathogenic variants in GJB1"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Dejerine-Sottas disease", "Family history of hereditary neuropathy", "Differentiation from other neuromuscular disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81523-0 ICD-10: G60.0 Clinical summary This test evaluates the GJB1 gene for pathogenic variants associated with Dejerine-Sottas disease.
TEST-4055 LITAF Gene Sequencing (CMT1C) Test This test identifies pathogenic variants in the LITAF gene associated with Charcot-Marie-Tooth disease type 1C (CMT1C).	Whole Blood (EDTA) or Buccal Swab	18–21 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the LITAF gene", "Single-nucleotide variants", "Small insertions and deletions", "Copy-number variations"] Parameters [] Preparation ["No fasting required", "Ensure child is well-hydrated for pediatric collection"] Indications ["Diagnosis of Charcot-Marie-Tooth disease type 1C (CMT1C)", "Family counseling for CMT1C", "Prognosis determination for CMT1C", "Therapeutic planning for CMT1C"] Measurement technique Confirm with laboratory Codes LOINC: 94219-9 ICD-10: G60.0 Clinical summary This test identifies pathogenic variants in the LITAF gene associated with Charcot-Marie-Tooth disease type 1C (CMT1C).
TEST-3999 MPZ Gene CMT1B Genetic Test This test evaluates the MPZ gene for pathogenic variants associated with Charcot-Marie-Tooth disease type 1B.	Peripheral Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants (SNVs, indels, CNVs) in the MPZ gene"] Parameters [] Preparation ["No fasting required", "Continue all prescribed medications", "Inform phlebotomist of anticoagulant use"] Indications ["Suspected Charcot-Marie-Tooth disease type 1B", "Evaluation of hereditary neuropathy"] Measurement technique Confirm with laboratory Codes LOINC: 82356-5 ICD-10: G60.0 Clinical summary This test evaluates the MPZ gene for pathogenic variants associated with Charcot-Marie-Tooth disease type 1B.
TEST-4100 MPZ Gene CMT4E Genetic Test This test identifies germline mutations in the MPZ gene associated with Charcot-Marie-Tooth disease type 4E.	Peripheral whole blood, extracted DNA, or FTA card (dried blood spot)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MPZ gene pathogenic variants", "CMT4E genetic mutations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Diagnosis of Charcot-Marie-Tooth disease type 4E", "Identification of MPZ gene mutations"] Measurement technique Confirm with laboratory Codes LOINC: 81327-2 ICD-10: G60.0 Clinical summary This test identifies germline mutations in the MPZ gene associated with Charcot-Marie-Tooth disease type 4E.
TEST-4042 MTMR2 Gene CMT4B1 Genetic Test This test evaluates the MTMR2 gene for mutations associated with Charcot-Marie-Tooth disease type 4B1.	Peripheral Whole Blood (EDTA tube) or Buccal Swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MTMR2 gene sequence", "Copy number variations in MTMR2 gene"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counseling session is mandatory"] Indications ["Diagnosis of Charcot-Marie-Tooth disease type 4B1", "Family planning for CMT4B1", "Clinical management guidance for CMT4B1"] Measurement technique Confirm with laboratory Codes LOINC: 83231-6 ICD-10: G60.0 Clinical summary This test evaluates the MTMR2 gene for mutations associated with Charcot-Marie-Tooth disease type 4B1.
TEST-4053 PRX Gene CMT4F Genetic Test This test evaluates the PRX gene for pathogenic variants associated with Charcot-Marie-Tooth disease type 4F (CMT4F). It utilizes next-generation sequencing (NGS) to detect single-...	Whole blood, extracted DNA, or one drop blood on FTA card	3–4 weeks (expedited reporting for urgent cases)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PRX gene", "Single-nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy-number variations (CNVs)"] Parameters [] Preparation ["A mandatory genetic counselling session must be completed prior to collection.", "No fasting is needed.", "Provide a detailed three-generation family history pedigree."] Indications ["Suspected Charcot-Marie-Tooth disease type 4F (CMT4F)", "Family history of CMT4F", "Need for definitive genetic diagnosis for management and counselling"] Measurement technique Confirm with laboratory Codes LOINC: 94233-7 ICD-10: G60.0 Clinical summary This test evaluates the PRX gene for pathogenic variants associated with Charcot-Marie-Tooth disease type 4F (CMT4F). It utilizes next-generation sequencing (NGS) to detect single-nucleotide variants, small insertions/deletions, and copy-number variations.
TEST-4093 SBF2 Gene CMT4B2 Genetic Test This test detects pathogenic variants, including point mutations, small indels, and copy number variations, within the SBF2 gene to diagnose Charcot-Marie-Tooth disease type 4B2.	EDTA whole blood (3–5 mL), extracted DNA (2 µg minimum), or FTA card blood spot	21–28 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SBF2 gene sequence", "Copy Number Variations (CNVs) in SBF2 gene", "Pathogenic variants in SBF2 gene"] Parameters [] Preparation ["Continue all prescribed medications unless instructed otherwise by your physician.", "Inform the phlebotomist if taking anticoagulant or antiplatelet medications."] Indications ["Individuals with clinical features suggestive of CMT4B2", "Family members of a confirmed CMT4B2 proband for carrier status or presymptomatic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 62342-6 ICD-10: G60.0 Clinical summary This test detects pathogenic variants, including point mutations, small indels, and copy number variations, within the SBF2 gene to diagnose Charcot-Marie-Tooth disease type 4B2.

Category overview

Charcot-Marie-Tooth Disease: overview

Coping with progressive muscle weakness, loss of sensation in the limbs, or high foot arches can be deeply unsettling, but securing precise genetic answers offers a clear pathway to targeted management. Representing an advanced subspecialty within our neurogenetics department, Charcot-Marie-Tooth (CMT) Disease testing evaluates your DNA for the specific inherited mutations that damage the peripheral nerves. By leveraging cutting-edge sequencing technology, this vital molecular screening helps classify the exact subtype of this complex neuropathy, safely guiding personalized physical therapy, orthopedic support, and proactive medical oversight. Highly regarded for neurological diagnostic excellence among top diagnostic labs in Dubai and the UAE, DNA Labs ensures absolute patient confidentiality, uncompromising analytical accuracy, and incredibly prompt reporting. Take control of your neurological health—book your Charcot-Marie-Tooth disease testing in UAE, arrange a secure clinical sample collection, or connect with our specialized medical 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.