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Respiratory exacerbation in a young adult with cystic fibrosis and tricuspid atresia
Tricuspid atresia (TAt) is a complex congenital heart defect (CHD) characterized by the absence of the tricuspid valve and right ventricular hypoplasia requiring surgery in childhood, the Fontan procedure. We present a case of a 21‐year‐old male with TAt and cystic fibrosis (CF), who underwent a Fon...
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| Vydáno v: | Respirol Case Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley & Sons, Ltd
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5879030/ https://ncbi.nlm.nih.gov/pubmed/29619223 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/rcr2.318 |
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