Outcome of a pregnant woman with polymorbiditys

Case report

Authors

  • Anne Dryelle de Sousa Henriques
  • Tallyta Miranda
  • Suzane Maria de Sousa Sá
  • Kassandra Ferreira Pessoa Oliveira

DOI:

https://doi.org/10.56102/afmo.2018.33

Keywords:

Gestation, Methylenetetrahydrofolate reductase, Hypothyroidism

Abstract

Objective: To report the outcome of pregnant women with hypothyroidism and methylenethohydrofolate reductase mutation (MTHFR) indicative of hereditary thrombophilia trait. Case report: WSR, 38 year-old, puerperal, G1P1A0 and with a history of pulmonary thromboembolism (PTE) a year ago. The exams diagnosed hypothyroidism and trait heterozygous hereditary thrombophilia. She also had extreme fatigue due to a diagnosis of anemia, a low insertion placenta and lactose intolerance. At 35 weeks, emergency cesarean section, without intercurrences with the fetus. Comments: It is understood the importance of prenatal consultations in an active search for morbidities that may cause intercurrences for pregnant women and the fetus, in addition to multidisciplinary follow-up to provide the outcome favorable to gestation.

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Published

2018-08-04

How to Cite

de Sousa Henriques, A. D., Miranda, T., de Sousa Sá, S. M., & Ferreira Pessoa Oliveira, K. (2018). Outcome of a pregnant woman with polymorbiditys: Case report. Annals of Olinda Medical School, 1(2), 50–51. https://doi.org/10.56102/afmo.2018.33

Issue

Vol. 1 No. 2 (2018)

Section

Case Reports

License

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