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.
Original language | English |
---|---|
Pages (from-to) | 381-383 |
Number of pages | 3 |
Journal | Pulmonary Circulation |
Volume | 6 |
Issue number | 3 |
DOIs | |
State | Published - 1 Sep 2016 |
Externally published | Yes |
Keywords
- BMPR2
- Pregnancy
- Pulmonary arterial hypertension
- Right ventricle