Multiple congenital visceral abnormalities as a rare cause of pulmonary arterial hypertension

Abstract Background Pulmonary arterial hypertension (PAH) is a rare, progressive disorder. PAH is caused by a wide spectrum of pathologies but the cause remains undetermined on many occasions and patients are classified in the idiopathic group. Case presentation Here we report a young woman with rar...

Full description

Bibliographic Details

Published in:	The Egyptian Heart Journal
Main Authors:	Parham Rabiee, Sedigheh Saedi
Format:	Article
Language:	English
Published:	SpringerOpen 2022-04-01
Subjects:	Congenital heart disease Pulmonary hypertension Mayer–Rokitansky–Küster–Hauser syndrome Abernethy malformation
Online Access:	https://doi.org/10.1186/s43044-022-00273-x