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...

書誌詳細
出版年:	The Egyptian Heart Journal
主要な著者:	Parham Rabiee, Sedigheh Saedi
フォーマット:	論文
言語:	英語
出版事項:	SpringerOpen 2022-04-01
主題:	Congenital heart disease Pulmonary hypertension Mayer–Rokitansky–Küster–Hauser syndrome Abernethy malformation
オンライン･アクセス:	https://doi.org/10.1186/s43044-022-00273-x

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