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Pulmonary arterial hypertension in hereditary hemorrhagic telangiectasia associated with ACVRL1 mutation: a case report
INTRODUCTION: Hereditary hemorrhagic telangiectasia is an autosomal dominant condition with an estimated prevalence of 1 in 5000. It is characterized by the presence of abnormalities of vascular structures, and may affect many organ systems, including the lungs, brain, spinal cord, gastrointestinal...
Autores principales: | Walsh, L. J., Collins, C., Ibrahim, H., Kerins, D. M., Brady, A. P., O Connor, T. M. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889686/ https://www.ncbi.nlm.nih.gov/pubmed/35232468 http://dx.doi.org/10.1186/s13256-022-03296-9 |
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