Loeys-Dietz syndrome in pregnancy: a case description and report of a novel mutation

Fetal Diagn Ther. 2009;26(1):35-7. doi: 10.1159/000236357. Epub 2009 Oct 10.

Abstract

Loeys-Dietz syndrome is a syndrome caused by heterozygous mutations in the genes encoding type 1 or 2 transforming growth factor-beta receptor (TGF-beta-R1/2). The obstetrical manifestations are risk of rupture of the gravid uterus and the arteries, either during pregnancy or in the immediate postpartum period, and damage to the vagina, perineum and the colon. We describe, for the first time, a new TGF-beta-R2 gene mutation in a family with several individuals who either had aortic rupture and dissection, sudden death or aortic root dilatation. The pregnancy was followed up and the baby was successfully delivered by a cesarean section at 34 weeks of gestation. The mother's recovery was uneventful and the baby was negative for the mutation on postnatal molecular testing. With appropriate supervision and early delivery by cesarean section, women with Loeys-Dietz syndrome can tolerate pregnancy and delivery without any adverse effect.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Cesarean Section
  • Diagnosis, Differential
  • Female
  • Humans
  • Infant, Newborn
  • Loeys-Dietz Syndrome / complications*
  • Loeys-Dietz Syndrome / genetics
  • Male
  • Marfan Syndrome / genetics
  • Mutation, Missense
  • Pregnancy
  • Pregnancy Complications*
  • Receptors, Transforming Growth Factor beta / genetics

Substances

  • Receptors, Transforming Growth Factor beta