Diagnostic options · UAE

ALS Genetic tests in Dubai & UAE

Compare available ALS Genetic 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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ALS Genetic test prices

Showing 1–5 of 5 matching tests.

ALS Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3788 CHGB Gene ALS Risk Factor Genetic Test This test evaluates the CHGB gene for pathogenic variants associated with an increased risk of developing Amyotrophic Lateral Sclerosis (ALS).	Peripheral Whole Blood	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CHGB gene", "Genetic susceptibility to ALS"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Individuals with a family history of ALS", "Assessment of genetic risk for ALS", "Genetic counselling for individuals concerned about ALS risk"] Measurement technique Confirm with laboratory Codes LOINC: 81208-0 ICD-10: Z13.89 Clinical summary This test evaluates the CHGB gene for pathogenic variants associated with an increased risk of developing Amyotrophic Lateral Sclerosis (ALS).
TEST-3813 FUS Gene ALS Type 6 Genetic Test This test evaluates the FUS gene for mutations associated with Amyotrophic Lateral Sclerosis Type 6 (ALS6).	Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FUS gene single-nucleotide variants", "Insertions", "Deletions", "Structural rearrangements", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue prescribed medication without consulting your neurologist."] Indications ["Diagnosis of familial ALS", "Confirmation of ALS Type 6", "Genetic counseling for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 83547-3 ICD-10: G12.21 Clinical summary This test evaluates the FUS gene for mutations associated with Amyotrophic Lateral Sclerosis Type 6 (ALS6).
TEST-3786 SETX Gene Amyotrophic Lateral Sclerosis Type 4 Genetic Test This test identifies pathogenic variants in the SETX gene, which are associated with juvenile-onset amyotrophic lateral sclerosis type 4 (ALS Type 4).	Whole Blood (EDTA), Extracted DNA (≥1 µg), or Dried Blood Spot (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 SETX gene"] Parameters [] Preparation ["No fasting required"] Indications ["Individuals with suspected juvenile-onset, slowly progressive motor neuron disease", "Family history of ALS Type 4", "Carrier testing for family members of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 94219-1 ICD-10: G12.21 Clinical summary This test identifies pathogenic variants in the SETX gene, which are associated with juvenile-onset amyotrophic lateral sclerosis type 4 (ALS Type 4).
TEST-3804 UBQLN2 Gene Analysis (Amyotrophic Lateral Sclerosis, X-Linked Juvenile & Adult-Onset) Genetic Test This genetic test identifies pathogenic variants in the UBQLN2 gene, which are associated with specific forms of amyotrophic lateral sclerosis (ALS). It helps confirm a diagnosis a...	Peripheral Whole Blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["UBQLN2 gene sequence", "Pathogenic variants in UBQLN2"] Parameters [] Preparation [] Indications ["Clinical suspicion of X-linked amyotrophic lateral sclerosis (ALS)", "Definitive molecular diagnosis for prognosis and family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 81265-2 ICD-10: G12.21 Clinical summary This genetic test identifies pathogenic variants in the UBQLN2 gene, which are associated with specific forms of amyotrophic lateral sclerosis (ALS). It helps confirm a diagnosis and assess familial risk.
TEST-3790 VAPB Gene Amyotrophic Lateral Sclerosis Type 8 (ALS8) Genetic Test This test detects pathogenic variants in the VAPB gene associated with autosomal dominant amyotrophic lateral sclerosis type 8.	Whole Blood (EDTA)	14-21 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 VAPB gene"] Parameters [] Preparation [] Indications ["Family history of amyotrophic lateral sclerosis", "Early-onset motor neuron disease", "Known VAPB variant in the family"] Measurement technique Confirm with laboratory Codes LOINC: 59027-5 ICD-10: G12.21 Clinical summary This test detects pathogenic variants in the VAPB gene associated with autosomal dominant amyotrophic lateral sclerosis type 8.

Category overview

ALS Genetic: overview

Facing a family history of progressive muscle weakness or motor neuron decline is incredibly daunting, but securing precise genetic answers provides empowering clarity for you and your loved ones. As a highly specialized offering within our neurogenetics department, ALS (Amyotrophic Lateral Sclerosis) Genetic testing evaluates your DNA for inherited mutations—such as those in the SOD1 or C9orf72 genes—known to cause familial forms of the disease. By leveraging cutting-edge diagnostic technology, this vital molecular screening helps assess your hereditary risks, offering the definitive data needed to safely guide proactive neurological monitoring, advanced clinical trial access, and specialized genetic counseling. Consistently trusted by neurologists across top diagnostic labs in Dubai and the UAE, DNA Labs guarantees strict patient confidentiality, exceptional analytical precision, and remarkably fast turnaround times. Take an informed step forward—book your ALS genetic testing in UAE, coordinate a comfortable home sample collection, or consult our dedicated 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.