| Literature DB >> 27683615 |
Maude Limoges1, David Langleben1, Benjamin D Fox2, Roberta Shear3, Paul Wieczorek4, Lawrence G Rudski1, Andrew M Hirsch1, Robert D Schlesinger1, Lyda Lesenko1.
Abstract
It is unclear whether pregnancy is a trigger or accelerant for idiopathic pulmonary arterial hypertension (PAH). Alternatively, its frequency close to the onset of symptoms and diagnosis in the idiopathic PAH population may represent a coincidence in a disease that predominates in young women. We describe a carrier of a BMPR2 gene mutation who had an uneventful first pregnancy but had aggressive PAH during her second pregnancy and now has ongoing heritable PAH. The possible role of pregnancy as a trigger in this vulnerable patient is discussed. Databases of patients with heritable PAH should be explored to see whether pregnancy is related to overt manifestation of the disease.Entities:
Keywords: BMPR2; pregnancy; pulmonary arterial hypertension; right ventricle
Year: 2016 PMID: 27683615 PMCID: PMC5019091 DOI: 10.1086/686993
Source DB: PubMed Journal: Pulm Circ ISSN: 2045-8932 Impact factor: 3.017