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A case of reversible pulmonary arterial hypertension associated with incontinentia pigmenti
Incontinentia pigmenti (IP) is a multisystemic disorder in which pulmonary arterial hypertension (PAH) is a severe and rarely reported association. The prognosis has been poor in reported cases. In our patient, IP was diagnosed during the neonatal period with a combination of cutaneous, ophthalmic,...
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| Publicado no: | Pulm Circ |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6131310/ https://ncbi.nlm.nih.gov/pubmed/30036148 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2045894018793983 |
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