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Pubertal development in rett syndrome deviates from typical females

  • Author(s): Killian, JT
  • Lane, JB
  • Cutter, GR
  • Skinner, SA
  • Kaufmann, WE
  • Tarquinio, DC
  • Glaze, DG
  • Motil, KJ
  • Neul, JL
  • Percy, AK
  • et al.

Published Web Location

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254166/
No data is associated with this publication.
Abstract

© 2014 Elsevier Inc. All rights reserved. BACKGROUND: Rett syndrome is a unique neurodevelopmental disorder, affecting approximately one in 10,000 live female births, most experiencing reduced growth. We characterized pubertal trajectories in females with Rett syndrome. We hypothesized that pubertal trajectory deviates fromthe general female populationwith early pubertal onset and delayed menarche. METHODS: Participants were individuals enrolled in the Rett Syndrome Natural History Study with clinical diagnosis of Rett syndrome or mutations in MECP2. Intervals to thelarche, adrenarche, and menarche were assessed by survival analysis; body mass index, mutation type, clinical severity, and pubertal milestone relationships were assessed by log-likelihood test; pathway synchrony (relationship between thelarche, adrenarche, and menarche) was assessed by chi-squared analysis. RESULTS: Compared with the general female population, more than 25% initiated puberty early, yet entered menarche later (median age 13.0 years). A total of 19% experienced delayed menarche. Median length of puberty, from thelarche to menarche, was 3.9 years. Higher body mass index correlated with earlier thelarche and adrenarche but not menarche; milder mutations correlated with earlier menarche; and milder clinical presentation correlated with earlier thelarche and menarche. Fifty-two percent entered puberty in synchrony, but different from the general population, 15% led with thelarche and 32% with adrenarche. CONCLUSIONS: Pubertal trajectories in Rett syndrome differ from general population, entering puberty early and reaching menarche later. Body mass index affects pubertal timing, but the relationship between specific mutations, clinical presentation, and underlying neuroendocrine pathology is less clear.

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