| Literature DB >> 33995573 |
Katharine E Thomas1, Jennifer Hogan2, Alex Pitcher3, Lucy Mackillop1, Edward Blair4, Charlotte J Frise1.
Abstract
Loeys-Dietz syndrome is a recently described condition which causes cardiovascular, craniofacial, neurocognitive and skeletal abnormalities due to mutations in components of the transforming growth factor-β signalling pathway. Associated vascular abnormalities include vessel tortuosity and an increased incidence of vascular dissection. Pregnancy increases the risk of aortic dissection compared to non-pregnant individuals and an underlying condition such as Loeys-Dietz syndrome increases this further. While aortic dissection is well described in pregnancy in Loeys-Dietz syndrome, some women can have uncomplicated deliveries, particularly when the risks of the condition are actively managed. Such pregnancies should be considered high-risk, and women should be counselled and managed accordingly. Here we describe two pregnancies in one woman, both with successful outcomes, followed by a summary of the key management principles.Entities:
Keywords: Loeys–Dietz syndrome; aortic dissection
Year: 2019 PMID: 33995573 PMCID: PMC8107958 DOI: 10.1177/1753495X19852819
Source DB: PubMed Journal: Obstet Med ISSN: 1753-495X