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Hereditary haemorrhagic telangiectasia with heritable pulmonary arterial hypertension.
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📄 Paper Details
Hereditary haemorrhagic telangiectasia with heritable pulmonary arterial hypertension.
Wei-Wei Zhu; Xiu-Zhang Lv; Wen-Huan Li
Abstract
Pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies most commonly seen in hereditary hemorrhagic telangiectasia (HHT), a condition associated with mutations in ENG, ACVRL1, SMAD4, or GDF2. In contrast, BMPR2 variants are well-established in heritable pulmonary arterial hypertension (PAH), but their relationship to PAVMs remains poorly understood. We report the case of a 41-year-old woman with an incidentally discovered PAVM, initially treated with embolization and subsequen...
Metadata
| quality_evaluation | {'agent': 'codex-slot-40', 'signals': {'pmid': '32457986', 'year': 2020, 'journal': 'European heart journal', 'usage_score': 0.5, 'abstract_present': False}, 'task_id': 'ebade91a-4f4c-4088-b7f0-9389b7 |
📊 Evidence Profile
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