Pulmonary arterial hypertension-associated genetic variants in combined post-capillary and pre-capillary pulmonary hypertension: a case report.
heart failure
mutations
pulmonary arterial hypertension
pulmonary circulation
risk factors
Journal
Pulmonary circulation
ISSN: 2045-8932
Titre abrégé: Pulm Circ
Pays: United States
ID NLM: 101557243
Informations de publication
Date de publication:
Historique:
received:
28
01
2021
accepted:
01
02
2021
entrez:
19
3
2021
pubmed:
20
3
2021
medline:
20
3
2021
Statut:
epublish
Résumé
Predisposing factors for the development of a pre-capillary component in pulmonary hypertension associated with left heart disease remain elusive. We report the case of a patient with persistent combined post-capillary and pre-capillary pulmonary hypertension after cardiac transplantation, in whom a rare
Identifiants
pubmed: 33738094
doi: 10.1177/2045894021996571
pii: 10.1177_2045894021996571
pmc: PMC7934041
doi:
Types de publication
Case Reports
Langues
eng
Pagination
2045894021996571Informations de copyright
© The Author(s) 2021.
Déclaration de conflit d'intérêts
Declaration of Conflicting Interests: Outside the submitted work: AB received consultancy fees from Amicus, Baeyer, Boehringer Ingelheim, Sanofi, Pfizer, and Alnylam; speaker fees from Pfizer, Sanofi, and Alnylam; and reports travel grants from Abbott, Pfizer, and Takeda. JLV received consultancy fees from Actelion, Bayer, Bial Portela, PhaseBio, Respira Therapeutics, United Therapeutics, and SoniVie and reports speaker fees and travel grants from Actelion, Acceleron, Bayer, Merck, Novartis, and United Therapeutics. LC reports travel grants from Sanofi and Pfizer. SC received an ERS PAH Short-Term Research Training Fellowship (STRTF 2014-5264) supported by an unrestricted grant by GSK and the international grant “Cesare Bartorelli” in 2014 funded by the Italian Society of Hypertension. CD and MA have nothing to disclose.
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