Hereditary Hemorrhagic Telangiectasia tests in Dubai & UAE

Compare available Hereditary Hemorrhagic Telangiectasia 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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Hereditary Hemorrhagic Telangiectasia test prices

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Hereditary Hemorrhagic Telangiectasia diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4536 ACVRL1 Gene (Hereditary Hemorrhagic Telangiectasia Type 2) Genetic Test This genetic test evaluates the ACVRL1 gene for pathogenic variants associated with Hereditary Hemorrhagic Telangiectasia Type 2 (HHT2).	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 ["ACVRL1 gene sequence", "Single Nucleotide Variants (SNVs)", "Small Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No fasting required", "Inform phlebotomist about anticoagulant/antiplatelet therapy", "Pre-test genetic counselling is mandatory"] Indications ["Diagnosis of HHT2 in symptomatic individuals", "Carrier screening in families with known ACVRL1 mutations", "Prenatal diagnosis", "Preimplantation genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 82588-6 ICD-10: I78.0 Clinical summary This genetic test evaluates the ACVRL1 gene for pathogenic variants associated with Hereditary Hemorrhagic Telangiectasia Type 2 (HHT2).
TEST-4517 ENG Gene Hereditary Hemorrhagic Telangiectasia Type 1 (HHT1) Genetic Test This test evaluates the ENG gene for pathogenic variants associated with Hereditary Hemorrhagic Telangiectasia Type 1 (HHT1). It identifies single-nucleotide changes, small inserti...	Peripheral Whole Blood or FTA Card 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 ENG gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNV)"] Parameters [] Preparation ["No fasting required", "No special preparation required"] Indications ["Diagnosis of HHT1 in symptomatic individuals", "Family cascade screening for HHT1", "Confirmation of HHT1 diagnosis based on clinical criteria"] Measurement technique Confirm with laboratory Codes LOINC: 93935-1 ICD-10: I78.0 Clinical summary This test evaluates the ENG gene for pathogenic variants associated with Hereditary Hemorrhagic Telangiectasia Type 1 (HHT1). It identifies single-nucleotide changes, small insertions/deletions, and copy number alterations within the gene.

Category overview

Hereditary Hemorrhagic Telangiectasia: overview

Confronting severe, recurrent nosebleeds, unexplained anemia, or the sudden discovery of vascular malformations in your lungs or brain requires immediate, highly specific diagnostic intervention. Representing an elite diagnostic tool in our Genetics services, Hereditary Hemorrhagic Telangiectasia (HHT) testing maps the ENG or ACVRL1 genes for inherited mutations that cause abnormal blood vessel formation (arteriovenous malformations). Utilizing state-of-the-art sequencing technology, this life-saving molecular screening helps confirm this dangerous vascular condition, offering the definitive data needed to safely guide critical cardiovascular and neurological imaging, targeted preventative surgeries, and proactive medical management. Consistently ranked among the premier diagnostic labs in the UAE for complex vascular diagnostics, DNA Labs ensures strict patient confidentiality, unparalleled diagnostic precision, and incredibly fast reporting. Protect your critical vascular infrastructure—book your HHT testing in UAE, arrange a secure clinical sample transfer, or consult our dedicated medical specialists.

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