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Pulmonary arterial hypertension: A rare yet fatal complication of Neurofibromatosis Type 1
Neurofibromatosis Type 1 (NF1) is an autosomal dominant genetic disorder with an incidence of approximately 1 in 4,000 live births ([1]). Pulmonary arterial hypertension (PAH) is a rare but extremely life-threatening complication associated with NF1. Timely recognition of this unusual and severe ass...
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| Publicat a: | Respir Med Case Rep |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6451192/ https://ncbi.nlm.nih.gov/pubmed/30997327 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2019.100832 |
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