Hereditary Neuropathy tests in Dubai & UAE

Compare available Hereditary Neuropathy 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

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Hereditary Neuropathy test prices

Showing 1–2 of 2 matching tests.

Hereditary Neuropathy diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4128 EGR2 Gene Dejerine-Sottas Disease Genetic Test This test analyzes the EGR2 gene for mutations associated with Dejerine-Sottas disease (HMSN Type III), a hereditary motor and sensory neuropathy.	Whole Blood (EDTA) or Extracted DNA or FTA Card Blood Spot	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 EGR2 gene", "Full coding region and splice sites of the EGR2 gene"] Parameters [] Preparation ["No fasting required", "No medication adjustment required unless directed by physician", "Provide detailed clinical history", "Attend genetic counseling session"] Indications ["Suspected Dejerine-Sottas disease based on clinical presentation", "Family history of hereditary motor and sensory neuropathy", "Need for definitive genetic diagnosis for treatment planning and genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 21663-4 ICD-10: G60.0 Clinical summary This test analyzes the EGR2 gene for mutations associated with Dejerine-Sottas disease (HMSN Type III), a hereditary motor and sensory neuropathy.
TEST-5373 SPTLC2 Gene Neuropathy, Hereditary Sensory and Autonomic Type 1C (HSAN1C) Genetic Test This test identifies pathogenic variants in the SPTLC2 gene, confirming a diagnosis of Hereditary Sensory and Autonomic Neuropathy Type 1C (HSAN1C).	Whole Blood (EDTA tube), Extracted DNA (minimum 1 µg), 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 SPTLC2 gene", "Serine palmitoyltransferase enzyme function"] Parameters [] Preparation ["No fasting required for whole blood collection", "Inform phlebotomist if on anticoagulant therapy"] Indications ["Clinical suspicion of HSAN1C", "Patients with progressive sensory neurodegeneration", "Patients with autonomic dysfunction"] Measurement technique Confirm with laboratory Codes LOINC: 101621-2 ICD-10: G60.8 Clinical summary This test identifies pathogenic variants in the SPTLC2 gene, confirming a diagnosis of Hereditary Sensory and Autonomic Neuropathy Type 1C (HSAN1C).

Category overview

Hereditary Neuropathy: overview

Coping with progressive muscle weakness, persistent numbness in the hands and feet, or distinct structural changes like high foot arches requires proactive, molecular insights to protect your long-term mobility. Integrated into our advanced neurogenetics department, Hereditary Neuropathy testing evaluates your DNA for the specific inherited mutations responsible for damaging peripheral nerves, such as those causing Charcot-Marie-Tooth disease. Utilizing cutting-edge sequencing technology, this expansive molecular screening helps pinpoint the exact subtype of your condition, safely guiding your healthcare provider in tailoring highly personalized physical therapy, customized orthopedic support, and proactive neurological oversight. Trusted for diagnostic excellence across the best diagnostic labs in the UAE, DNA Labs ensures strict patient confidentiality, uncompromising diagnostic precision, and remarkably fast reporting. Take control of your neurological health—book your hereditary neuropathy testing in UAE, arrange a secure clinical sample collection, or reach out to our specialized medical professionals.

Before booking

Use the test details as a conversation starter

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.