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Pulmonary hypertension associated with congenital heart disease; clinical decision scenario
Pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD) is one type under group 1 PH. Undiagnosed or delayed diagnosis of significant CHD might lead to significant PAH and at the end might lead to Eisenmenger syndrome. We could expect the degree of PAH in patients with CHD...
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| Izdano u: | Respir Med Case Rep |
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| Glavni autori: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Elsevier
2020
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7683341/ https://ncbi.nlm.nih.gov/pubmed/33294357 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2020.101286 |
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