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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Detalhes bibliográficos
Publicado no:Respir Med Case Rep
Main Authors: Rojas, Melanie, Mubarik, Ateeq, Henderson, Elizabeth Ann, Agha, Fatima, Chauhan, Lakshpaul, Iqbal, Arshad Muhammad, Vaziri, Ali, Muddassir, Salman
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
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Article
Acesso em linha: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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