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Pregnancy Outcomes in Congenital Myasthenie Syndrome (POCoMS)

I

Institut de Myologie, France

Status

Completed

Conditions

Congenital Myasthenic Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT01474980
2010-A00495-34

Details and patient eligibility

About

This is a retrospective study that follows the clinical evolution, the pregnancy and the post-partum perioad of female patients with Congenital Myasthenic Syndrome.

Full description

The aim of this study is to better understand the action of hormonal factors that are presumably incriminated for the fluctuation of the disease. The investigators would also like to better adress the issues of women with Congenital Myasthenic Syndrome, who desire a pregnancy : the possibility of decompensation, the problems that can arise during the course of the childbearing, the risk of foetal malformations.

Enrollment

25 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult women
  • Congenital myastenic syndrome genetically confirmed or with clinical compatible and electrophysiological evidence
  • Written consent

Exclusion criteria

  • Neurological or general pathology occurs significantly with the initiation and conduct of a pregnancy.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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