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...

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Detalles Bibliográficos
Autores principales: Walsh, L. J., Collins, C., Ibrahim, H., Kerins, D. M., Brady, A. P., O Connor, T. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
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

Internet

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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