Hereditary Spastic Paraplegia tests in Dubai & UAE

Compare available Hereditary Spastic Paraplegia 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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Listed price range

2,800.00 AED

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Hereditary Spastic Paraplegia test prices

Showing 1–4 of 4 matching tests.

Hereditary Spastic Paraplegia diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5796 ARL6IP1 Gene SPG61 Genetic Test This test detects pathogenic variants in the ARL6IP1 gene, confirming a diagnosis of hereditary spastic paraplegia type 61 (SPG61).	Peripheral Whole Blood or FTA Card	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 ARL6IP1 gene", "Full gene coverage via Next-Generation Sequencing"] Parameters [] Preparation ["No specific fasting required.", "No medication or diet modifications needed prior to sample collection."] Indications ["Diagnosis of hereditary spastic paraplegia type 61 (SPG61)", "Family risk assessment", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 81409-9 ICD-10: G11.4 Clinical summary This test detects pathogenic variants in the ARL6IP1 gene, confirming a diagnosis of hereditary spastic paraplegia type 61 (SPG61).
TEST-5682 C12ORF65 Gene SPG55 Genetic Test This test identifies pathogenic variants in the C12ORF65 gene associated with hereditary spastic paraplegia type 55 (SPG55).	Whole Blood (EDTA), 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 C12ORF65 gene coding region", "Coverage of all coding exons & splice junctions"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session"] Indications ["Individuals with progressive lower-limb spasticity", "Positive family history of hereditary spastic paraplegia", "Carrier screening", "Unexplained neurological performance decline (authorized by DHA-licensed neurologist)"] Measurement technique Confirm with laboratory Codes LOINC: 81657-5 ICD-10: G11.4, Z84.0, Z13.85 Clinical summary This test identifies pathogenic variants in the C12ORF65 gene associated with hereditary spastic paraplegia type 55 (SPG55).
TEST-5792 NIPA1 Gene (SPG6) Next‑Generation Sequencing DNA Test This test identifies pathogenic variants in the NIPA1 gene associated with autosomal dominant hereditary spastic paraplegia type 6.	Whole Blood (EDTA), Extracted DNA, or 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 NIPA1 gene"] Parameters [] Preparation [] Indications ["Suspected Hereditary Spastic Paraplegia Type 6 (SPG6)", "Family history of SPG6"] Measurement technique Confirm with laboratory Codes LOINC: 94231-5 ICD-10: G11.4 Clinical summary This test identifies pathogenic variants in the NIPA1 gene associated with autosomal dominant hereditary spastic paraplegia type 6.
TEST-5660 SLC33A1 Gene (SPG42) Genetic Test This genetic test identifies pathogenic variants in the SLC33A1 gene associated with hereditary spastic paraplegia type 42 (SPG42).	Whole Blood (EDTA) or 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 SLC33A1 gene", "Copy Number Variations (CNVs) in SLC33A1"] Parameters [] Preparation [] Indications ["Diagnostic workup of spastic paraplegia", "Family risk stratification and counselling", "Proactive genetic insight for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 96799-3 ICD-10: G11.4 Clinical summary This genetic test identifies pathogenic variants in the SLC33A1 gene associated with hereditary spastic paraplegia type 42 (SPG42).

Category overview

Hereditary Spastic Paraplegia: overview

Dealing with the gradual onset of severe leg stiffness, progressive muscle weakness, and spasticity can be an exhausting diagnostic journey, but finding the exact biological root offers a clear path to targeted management. Representing a critical diagnostic tool in our advanced neurogenetics services, Hereditary Spastic Paraplegia (HSP) testing meticulously maps your DNA to identify the specific inherited mutations that degenerate the upper motor neurons in the spinal cord. Utilizing advanced sequencing technology, this vital molecular profiling ends the diagnostic guesswork, offering the definitive data necessary to safely guide highly personalized antispasmodic therapies, customized physical rehabilitation, and proactive neurological care. Consistently trusted by neurologists across top diagnostic labs in the UAE, DNA Labs ensures strict patient confidentiality, exceptional diagnostic accuracy, and prompt, reliable reporting. Empower your neurological resilience—book your hereditary spastic paraplegia testing in UAE, arrange a secure clinical sample transfer, or connect with our specialized medical team.

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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.