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Loeys–Dietz syndrome in pregnancy.

Authors :
Thomas, Katharine E
Hogan, Jennifer
Pitcher, Alex
Mackillop, Lucy
Blair, Edward
Frise, Charlotte J
Source :
Obstetric Medicine (1753-495X); Mar2021, Vol. 14 Issue 1, p42-45, 4p
Publication Year :
2021

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1753495X
Volume :
14
Issue :
1
Database :
Complementary Index
Journal :
Obstetric Medicine (1753-495X)
Publication Type :
Academic Journal
Accession number :
150211146
Full Text :
https://doi.org/10.1177/1753495X19852819