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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Detalles Bibliográficos
Autores principales: Rojas, Melanie, Mubarik, Ateeq, Henderson, Elizabeth Ann, Agha, Fatima, Chauhan, Lakshpaul, Iqbal, Arshad Muhammad, Vaziri, Ali, Muddassir, Salman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451192/
https://www.ncbi.nlm.nih.gov/pubmed/30997327
http://dx.doi.org/10.1016/j.rmcr.2019.100832

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451192/
https://www.ncbi.nlm.nih.gov/pubmed/30997327
http://dx.doi.org/10.1016/j.rmcr.2019.100832

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