ArticleCureus2026
Images in Medicine: Recognizing Hereditary Hemorrhagic Telangiectasia Through Mucocutaneous Findings and Its Management Challenges.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
5 authors.
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Abstract
Hereditary hemorrhagic telangiectasia, or Osler-Weber-Rendu syndrome, is a rare autosomal dominant vascular disorder characterized by dysregulated angiogenesis due to abnormalities in the transforming growth factor-β (TGF-β)/bone morphogenetic protein (BMP) signaling pathway that result in mucocutaneous telangiectasias and visceral arteriovenous malformations, leading to recurrent bleeding and multisystem involvement. This image-based case highlights characteristic mucocutaneous telangiectasias and illustrates the challenges of long-term disease management, including recurrent hospitalizations and limited durability of vascular interventions. The case emphasizes the importance of coordinated outpatient care and consideration of targeted therapies to reduce morbidity and bleeding recurrence.
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