Marfan syndrome and twin pregnancy. Case report

Authors

  • Carolina García Pumasunta Posgrado de Ginecología, Pontificia Universidad Católica del Ecuador
  • Alejandro Mayorga Garcés Especialista en Gastroenterología, Hospital General Docente Ambato, Ecuador
  • Fausto Viteri Mejía Especialista en Ginecología, Hospital Gineco-Obstétrico Isidro Ayora, Ecuador

DOI:

https://doi.org/10.31403/rpgo.v66i2193

Abstract

Marfan syndrome is a hereditary disorder of the connective tissue. Pregnant women who suffer from this syndrome have an increased risk of cardiac complications when the aortic diameter is greater than 40 mm. We present the case of a woman with twin pregnancy and preeclampsia and late diagnosis of Marfan syndrome. We discuss the need for early diagnosis, preconception counseling and multidisciplinary management in this type of pathology.

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Published

2019-06-27

How to Cite

García Pumasunta, C., Mayorga Garcés, A., & Viteri Mejía, F. (2019). Marfan syndrome and twin pregnancy. Case report. The Peruvian Journal of Gynecology and Obstetrics, 65(3), 345–348. https://doi.org/10.31403/rpgo.v66i2193

Issue

Section

Casos Clínicos

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