Isolated Pulmonary Arteriovenous Malformations Associated With BMPR2 Pathogenic Variants

Kularatne, M; Eyries, M; Savale, L; Humbert, M; Montani, D

Montani, D (通讯作者),Univ Paris Saclay, Fac Med, Paris, France.;Montani, D (通讯作者),Hop Bicetre, AP HP, Pulm Hypertens Natl Referral Ctr, Dept Resp & Intens Care Med, DMU 5 Thorinno, Le Kremlin Bicetre, France.;Montani, D (通讯作者),INSERM, Hop Marie Lannelongue, UMR S 999, Pulm Hypertens Pathophysiol & Novel Therapies Hop, Le Plessis Robinson, France.

CHEST, 2023; 164 (2): E23

Abstract

Heritable pulmonary arterial hypertension (PAH) is an uncommon cause of PAH and is associ-ated most frequently with pathogenic variants of BMPR2. Prio......

Full Text Link