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Rare Course of Bilateral Congenital Diaphragmatic Hernia Treated Thoracoscopically—Case Report
We present a rare case of metachronous bilateral congenital diaphragmatic hernia (CDH) in a newborn with additional malformations: macroglossia, pectus excavatum, and confirmed Simpson-Golabi-Behmel syndrome. We performed a successful thoracoscopic subsequent repair with a patch of the bilateral typ...
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| Publicat a: | Front Pediatr |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7200980/ https://ncbi.nlm.nih.gov/pubmed/32411638 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2020.00209 |
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