Congenital Myasthenic Syndromes and Pregnancy Outcome

Authors

  • Firmina Sambayeta Department of Neurology / Centro Hospitalar Universitário do Porto, Portugal https://orcid.org/0000-0002-0078-2407
  • Luísa Sousa Department of Neurology / Centro Hospitalar Universitário do Porto, Portugal; Centro Hospitalar de Entre o Douro e Vouga, Santa Maria da Feira, Portugal
  • Luís Ribeiro Department of Neurology / Hospital Pedro Hispano - Unidade Local de Saúde de Matosinhos, Matosinhos, Portugal
  • Sara Duarte Department of Neurology / Centro Hospitalar Universitário do Porto, Portugal
  • Carla Silva Pinto Department of Obstetrics and Gynaecology / Centro Materno-Infantil do Norte, Centro Hospitalar Universitário do Porto, Porto, Portugal
  • João Martins Electromyography laboratory, MedicilLisboa, Lisboa, Portugal
  • Ernestina Santos Department of Neurology / Centro Hospitalar Universitário do Porto, Portugal; Unit for Multidisciplinary Research in Biomedicine, Instituto de Ciências Biomédicas Abel Salazar (ICBAS) da Universidade do Porto, Portugal

DOI:

https://doi.org/10.46531/sinapse/CC/210072/2022

Keywords:

Myasthenic Syndromes, Congenital, Pregnancy Complications

Abstract

Congenital myasthenic syndromes (CMS) are genetic conditions characterized by dysfunction of the neuromuscular transmission. There is limited data on pregnancy safety in myasthenia gravis for both mother and child. Retrospective study on pregnant CMS patients who were followed in two tertiary hospitals and their clinical data was analyzed. Sixteen pregnancies from 9 patients with CMS and history of pregnancy were included: one had CHAT, two had DOK-7 and six had CHRNE mutations. Previous reports showed that pregnancy can exacerbate the clinical manifestations of CMS. There are no specific recommendations for the disease during pregnancy. Our work adds sixteen pregnancies of women with CMS, without major complications for the mothers or newborns, except in one woman, with a CHAT mutation, who had significant worsening of her symptoms during pregnancy and post-partum period. The follow-up results of these women by a multidisciplinary team resulted in better outcomes.

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References

Stephen H. Roblin et al. Anesthetic considerations for Myasthenia Gravis and Pregnancy. Anesth Analg. 1978;67:441-7. doi: 10.1213/00000539-197807000-00013.

Amanda C. Guidon, E. Wayne Massey. Neuromuscular disorders in pregnancy. Neurol Clin. 2012; 30:889-911. doi:10.1016/j.ncl.2012.04.002.

Servais L, Baudoin H, Zehrouni K, Richard P, Sternberg D, Fournier E, et al. Pregnancy in congenital myasthenic syndrome. J Neurol. 2013; 260: 815-19. doi:10.1007/s00415-012-6709-x.

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Published

2024-04-20

How to Cite

1.
Sambayeta F, Sousa L, Ribeiro L, Duarte S, Silva Pinto C, Martins J, et al. Congenital Myasthenic Syndromes and Pregnancy Outcome. Sinapse [Internet]. 2024 Apr. 20 [cited 2024 Nov. 21];22(1):29-33. Available from: https://sinapse.pt/index.php/journal/article/view/75

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Section

Case Reports

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