Hereditary Hemorrhagic Telangiectasia

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.