463
Views
7
CrossRef citations to date
0
Altmetric
Original Article

Prenatal care and labor in patients with mesenchimal dysplasias (Marfan syndrome, Ehlers–Danlos syndrome, hereditary hemorrhagic telangiectasia)

, , , , &
Pages 373-379 | Received 05 Apr 2018, Accepted 21 Jun 2018, Published online: 06 Sep 2018

References

  • Abdalla SA, Geisthoff UW, Bonneau D, et al. Visceral manifestations in hereditary haemorrhagic telangiectasia type 2. J Med Genet. 2003;40(7):494–502.
  • Borck G, Beighton P, Wilhelm C, et al. Arterial rupture in classic Ehlers–Danlos syndrome with COL5A1 mutation. Am J Med Genet A. 2010;152A(8):2090–2093.
  • Emmanuel Y, Thorne SA. Heart disease in pregnancy. Best Pract Res Clin Obstet Gynaecol. 2015;29(5):579–597.
  • Guntupalli KK, Karnad DR, Bandi V, et al. Critical illness in pregnancy: part II: common medical conditions complicating pregnancy and puerperium. Chest. 2015;148(5):1333–1345.
  • Hassan N, Patenaude V, Oddy L, et al. Pregnancy outcomes in Marfan syndrome: a retrospective cohort study. Am J Perinatol. 2015;30(2):123–130.
  • Inocêncio G, Braga A, Lima T, et al. Osler-Weber-Rendu syndrome during pregnancy. BMJ Case Rep. 2013;2013:bcr2013009792.
  • Kim WH, Bae J, Choi SW, et al. Stanford type A aortic dissection in a patient with Marfansyndrome during pregnancy: a case report. Korean J Anesthesiol. 2016;69(1):76–79.
  • Palmquist M, Pappas JG, Petrikovsky B, et al. Successful pregnancy outcome in Ehlers–Danlos syndrome, vascular type. J Matern Fetal Neonatal Med. 2009;22(10):924–927.
  • Smok DA. Aortopathy in pregnancy. Semin Perinatol. 2014;38(5):295–303.
  • Combeer EL, Combeer AD. A rare cause of maternal death: liver and inferior vena cava rupture due to previously undiagnosed Ehlers-Danlos Syndrome type IV. Eur J Anaesthesiol. 2008;25(9):765–767.
  • Cox DA, Ginde S, Kuhlmann RS, et al. Management of the pregnant woman with Marfan syndrome complicated by ascending aorta dilation. Arch Gynecol Obstet. 2014;290(4):797–802.
  • Jakobi P, Weiner Z, Best L, et al. Hereditary hemorrhagic telangiectasia with pulmonary arteriovenous malformations. Obstet Gynecol. 2001;97(5 Pt 2):813–814.
  • Master M, Day G. Acute aortic dissection in pregnancy in a woman with undiagnosed Marfan syndrome. Case Rep Obstet Gynecol. 2012;2012:490169.
  • Muiño Mosquera L, De Backer J. Managing aortic aneurysms and dissections during pregnancy. Expert Rev Cardiovasc Ther. 2015;13(6):703–714.
  • Preiss M, Hösli I, Holzgreve W, et al. Aortic dissection in pregnancy in Marfan syndrome-case report and treatment concept. Z Geburtshilfe Neonatol. 2001;205(3):110–113.
  • Shovlin CL. Pulmonary arteriovenous malformations. Am J Respir Crit Care Med. 2014;190(11):1217–1228.
  • Swietlik E, Doboszynska A. Recurrence of arterio-venous malformations with life-threatening complications in a pregnant woman with hereditary teleangiectasia. J Physiol Pharmacol. 2008;59(6):683–688.
  • Uchida T, Ogino H, Ando M, et al. Aortic dissection in pregnant woman with the Marfan syndrome. Kyobu Geka. 2002;55(8 Suppl):693–696.
  • Yang G, Peng W, Zhao Q, et al. Aortic dissection in women during the course of pregnancy or puerperium: a report of 11 cases in central south China. Int J Clin Exp Med. 2015;8(7):11607–11612.
  • Yang Z, Yang S, Wang F, et al. Acute aortic dissection in pregnant women. Gen Thorac Cardiovasc Surg. 2016;64(5):283–285.
  • Coulon C. Thoracic aortic aneurysms and pregnancy. Presse Med. 2015;44(11):1126–1135.
  • Erez Y, Ezra Y, Rojansky N. Ehlers-Danlos type IV in pregnancy. Fetal Diagn Ther. 2008;23(1):7–9.
  • de Gussem EM, Lausman AY, Beder AJ, et al. Outcomes of pregnancy in women with hereditary hemorrhagic telangiectasia. Obstet Gynecol. 2014;123(3):514–520.
  • Khurshid I, Downie GH. Pulmonary arteriovenous malformation. Postgrad Med J. 2002;78(918):191–197.
  • Iqbal M, Rossoff LJ, Steinberg HN, et al. Pulmonary arteriovenous malformations: a clinical review. Postgrad Med J. 2000;76(897):390–394.
  • Naud K, Horne G, Van den Hof MA. A woman with marfan syndrome in pregnancy: managing high vascular risk with multidisciplinary care. J Obstet Gynaecol Can. 2015;37(8):724–727.
  • Takahashi H, Matsubara S, Saito K, et al. Good obstetric outcome after embolisation of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia: planned pregnancy may also be important in this condition. Aust NZ J Obstet Gynaecol. 2014;54(2):191.
  • Wallace GM, Shovlin CL. A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1. Thorax. 2000;55(8):685–690.
  • Okamoto M, Hayatsu K, Tomita M, et al. [Continuous epidural analgesia with intensive monitoring of cardiovascular system for vaginal delivery in a patient with Marfan’s syndrome]. Masui. 2002;51(8):916–920.
  • Murray ML, Pepin M, Peterson S, et al. Pregnancy-related deaths and complications in women with vascular Ehlers–Danlos syndrome. Genet Med. 2014;16(12):874–880.
  • Wanga S, Silversides C, Dore A, et al. Pregnancy and thoracic aortic disease: managing the risks. Can J Cardiol. 2016;32(1):78–85.
  • Figueiredo S, Martins E, Lima MR, et al. Cardiovascular manifestations in Marfansyndrome. Rev Port Cardiol. 2001;20(12):1203–1218.
  • Kim SW, Kim D, Hong JM. Acute aortic dissection in pregnancy with the Marfan syndrome. Korean J Thorac Cardiovasc Surg. 2014;47(3):291–293.
  • Koh MB, Hunt BJ. The management of perioperative bleeding. Blood Rev. 2003;17(3):179–185.
  • Köhler F, Fotuhi P, Baumann G. Pregnancy and congenital heart defects. Z Kardiol. 2001;90(4):30–35.
  • Lambaudie E, Depret-Mosser S, Occelli B, et al. Marfan syndrome and pregnancy. Apropos of 4 cases. Gynecol Obstet Fertil. 2002;30(7–8):567–575.
  • Omnes S, Jondeau G, Detaint D, et al. Pregnancy outcomes among women with Marfan syndrome. Int J Gynecol Obstet. 2013;122(3):219–223.
  • Rahman J, Rahman FZ, Rahman W, et al. Obstetric and gynecologic complications in women with Marfan syndrome. J Reprod Med. 2003;48(9):723–728.
  • Westhoff-Bleck M, Hilfiker-Kleiner D. Marfan syndrome and pregnancy:monitoring and management. Eur Heart J. 2015;36(18):1066–1067.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.