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Dysautonomic Phenotype in Male Patients With MECP2 Mutation

NCT04502199 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2020-08-06

No results posted yet for this study

Summary

Dysautonomic signs are well known among girls with a Rett Syndrom. Rett syndrom is caused by a MECP2 mutation in 95% of cases. We want to search dysautonomic signs among boys with a MECP2 mutations because they are less studied than the girls and they have more varied phenotypes.

Conditions

  • MECP2-Related Severe Neonatal Encephalopathy
  • Dysautonomia
  • Masculinity

Interventions

OTHER

non interventional study

observational study

Sponsors & Collaborators

  • University Hospital, Brest

    lead OTHER

Eligibility

Max Age
16 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-15
Primary Completion
2021-01-13
Completion
2021-01-13

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04502199 on ClinicalTrials.gov