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,...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2018-09-01
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Series: | Pulmonary Circulation |
Online Access: | https://doi.org/10.1177/2045894018793983 |