Advanced search
Publication Cover
The Journal of Maternal-Fetal & Neonatal Medicine Volume 31, 2018 - Issue 13
Submit an article Journal homepage
317
Views
1
CrossRef citations to date
0
Altmetric
Original Article

Pregnancy and mesenchimal dysplasias (Marfan syndrome, Ehlers-Danlos syndrome, hereditary hemorrhagic telangiectasia)

L. S. RadetskayaI.M. Sechenov First Moscow State Medical University of the Public Health Ministry of the Russian Federation, Moscow, Russia
,
A. D. MakatsariyaI.M. Sechenov First Moscow State Medical University of the Public Health Ministry of the Russian Federation, Moscow, RussiaCorrespondence[email protected]
,
V. O. BitsadzeI.M. Sechenov First Moscow State Medical University of the Public Health Ministry of the Russian Federation, Moscow, Russia
&
J. K. KhizroevaI.M. Sechenov First Moscow State Medical University of the Public Health Ministry of the Russian Federation, Moscow, Russia
Pages 1768-1776 | Received 17 Apr 2017, Accepted 02 May 2017, Published online: 13 Jun 2017

References

  • Fomina IG, Makarov IE, Prokof’eva EB. Klinich. Meditsina. 2001;79:52–55.
  • Andelfinger G, Shirali GS, Raunikar RA, et al. Functional pulmonary atresia in neonatal Marfan’s syndrome: successful treatment with inhaled nitric oxide. Pediatr Cardiol. 2001;22:525–526.
  • Von Kodolitsch Y, Raghunath M, Nienaber CA. Marfan syndrome: prevalence and natural course of cardiovascular manifestations. Z Kardiol. 1998;87:150–160.
  • Toudjarska I, Kilpatrick MW, Lembessis P, et al. Novel approach to the molecular diagnosis of Marfan syndrome: application to sporadic cases and in prenatal diagnosis. Am J Med Genet. 2001;99:294–302.
  • Colman JM, Sermer M, Seaward PG, et al. Congenital heart disease in pregnancy. Cardiol Rev. 2000;8:166–173.
  • Dean JC. Management of Marfan syndrome. Heart. 2002;88:97–103.
  • Simpson LL, Athanassious AM, D'Alton ME. Marfan syndrome in pregnancy. Curr Opin Obstet Gynecol. 1997;9:337–341.
  • Lambaudie E, Depret-Mosser S, Occelli B, et al. Marfan syndrome and pregnancy. Apropos of 4 Cases. Gynecol Obstet Fertil. 2002;30:567–575.
  • Loeys B, Nuytinck L, Van Acker P, et al. Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS). Prenat Diagn. 2002;22:22–28.
  • Child AH. Marfan syndrome-current medical and genetic knowledge: how to treat and when. J Card Surg. 1997;12:131–135. discussion 135–6.
  • Moodie DS. Diagnosing Marfan syndrome is still based on clinical characteristics. Cleve Clin J Med. 1998;65:176. 179-81.
  • Paternoster DM, Santarossa C, Vettore N, et al. Obstetric complications in Marfan’s syndrome pregnancy. Minerva Ginecol. 1998;50:441–443.
  • Akashi H, Tayama K, Fujino T, et al. Surgical treatment for acute type A aortic dissection in pregnancy: a case of aortic root replacement just after Cesarean section. Jpn Circ J. 2000;64:729–730.
  • Mayet J, Steer P, Somerville J. Marfan syndrome, aortic dilatation, and pregnancy. Obstet Gynecol. 1998;92:713.
  • Jondeau G, Nataf P, Belarbi A, et al. Aortic dissection at 6 months gestation in a women with Marfan’s syndrome. Masui. 2002;51:916–920.
  • Preiss M, Hosli I, Holzgreve W, et al. Aortic dissection in pregnancy in Marfan syndrome–case report and treatment concept. Z Geburtshilfe Neonatol. 2001;205:110–113.
  • Aburawi EH, O'Sullivan J, Hasan A. Marfan’s syndrome: a review. Hosp Med. 2001;62:153–157.
  • Von Kodolitsch Y, Raghunath M, Nienaber CA. Marfan syndrome: strategies of interdisciplinary care. Dtsch Med Wochenschr. 1998;123:21–25.
  • Uchida T, Ogino H, Ando M, et al. Aortic dissection in pregnant woman with the Marfan syndrome. Kyobu Geka. 2002;55:693–696.
  • Rahman J, Rahman FZ, Rahman W, et al. Obstetric and gynecologic complications in women with Marfan syndrome. J Reprod Med. 2003;48:723–728.
  • Milewicz DM. Molecular genetics of Marfan syndrome and Ehlers-Danlos type IV. Curr Opin Cardiol. 1998;13:198–204.
  • Burrows NP. The molecular genetics of the Ehlers-Danlos Syndrome. Clin Exp Dermatol. 1999;24:99–106.
  • Heather NY, Walker LC. Mutations in the lysil hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers-Danlos syndrome type VI. Mol Genet Metab. 2002;71:212–224.
  • Matsubara S, Mandzia JL, ter Brugge K, et al. Angiographic and clinical characteristics of patients with cerebral arteriovenous malformations associated with hereditary hemorrhagic telangiectasia. Am J Neuradiol. 2000;21:1016–1020.
  • Abdalla SA, Pece-Barbara N, Vera S, et al. Analysis of ALK-1 and endoglin in newborns from families with hereditary hemorrhagic telangiectasia type 2. Hum Mol Genet. 2000;9:1227–1237.
  • Abdalla SA, Geithoff UW, Bonneau D, et al. Visceral manifestations in hereditary hemorrhagic telangiectasia type 2. J Med Genet. 2003;40:494–502.
  • Guttmaher AE, Marchuk DA, White R. Hereditary hemorrhagic telangiectasia. N Engl J Med. 1995;333:918–925.
  • Jakobi P, Weiner Z, Best L, et al. Hereditary hemorrhagic telangiectasia with pulmonary arteriovenous malformations. Obstet Gynecol. 2001;97:813–814.
  • Shovlin CL, Leterte M. Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms. Thorax. 1999;54:714–729.
  • Khurshid I, Downie GH. Pulmonary arteriovenous malformation. Postgrad Med J. 2002;78:191–197.
  • Mobeen I, Rossoff LJ. Pulmonary arteriovenous malformations: a clinical review. Postgrad Med J. 2000;76:390–394.
  • Shovlin CL, Winstock AR, Peters AM, et al. Medical complications of pregnancy in hereditary haemorrhagic telangiectasia. QJM. 1995;88:879–887.

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:

Order Reprints Request Corporate Permissions

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:

Request Academic Permissions

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.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.