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Published in 2025 at "BMJ Case Reports"
DOI: 10.1136/bcr-2025-265940
Abstract: Hereditary haemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a rare autosomal dominant disorder characterised by abnormal blood vessel formation, leading to recurrent epistaxis, mucocutaneous telangiectasias and arteriovenous malformations. The diagnosis is clinically based…
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Keywords:
skin colour;
colour dermoscopic;
hereditary haemorrhagic;
telangiectasia ... See more keywords