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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Detalles Bibliográficos
Autores principales: Atallah, Veronique, Meot, Mathilde, Kossorotoff, Manoelle, Galmiche-Rolland, Louise, Lardeux, Claude, Neven, Benedicte, Bodemer, Christine, Bonnet, Damien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131310/
https://www.ncbi.nlm.nih.gov/pubmed/30036148
http://dx.doi.org/10.1177/2045894018793983

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131310/
https://www.ncbi.nlm.nih.gov/pubmed/30036148
http://dx.doi.org/10.1177/2045894018793983

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