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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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Detalhes bibliográficos
Principais autores: Veronique Atallah, Mathilde Meot, Manoelle Kossorotoff, Louise Galmiche-Rolland, Claude Lardeux, Benedicte Neven, Christine Bodemer, Damien Bonnet
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley 2018-09-01
coleção:Pulmonary Circulation
Acesso em linha:https://doi.org/10.1177/2045894018793983
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