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Endothelial to Mesenchymal Transition in an HHT-like pediatric case of Multiple Pulmonary Arteriovenous Malformations

2024-04-27

Abstract excerpt

Pulmonary arteriovenous malformations (PAVMs) are vascular anomalies resulting in abnormal connection between pulmonary arteries and veins. In 80% of cases, PAVMs are present from birth, but clinical manifestations are rarely seen in childhood. These congenital malformations are typically associated with Hereditary Hemorrhagic Telangiectasia (HHT), a rare disease that affects 1 in 5,000/8,000 individuals. HHT dise...

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Literature Corpus work
1f724cb6-a05c-5ff6-ae33-7e9dbcc94ccc
DOI
10.20944/preprints202404.1781.v1
Open publication

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Endothelial to Mesenchymal Transition in an HHT-like pediatric case of Multiple Pulmonary Arteriovenous MalformationsDOI 10.20944/preprints202404.1781.v1
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