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Congenital extrahepatic portocaval malformation: Rare but potentially treatable cause of pulmonary hypertension
OBJECTIVE: Abernethy malformation (congenital extrahepatic portosystemic shunt) is a rare anomaly of the splanchnic venous system. Though rare, it is an important cause of pulmonary artery hypertension (PAH) which is often missed. All patients with PAH should be carefully evaluated for presence of A...
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| Published in: | Indian Heart J |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Elsevier
2021
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7961257/ https://ncbi.nlm.nih.gov/pubmed/33714417 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ihj.2020.12.015 |
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