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Puberty and pubertal growth dynamics in children with idiopathic short stature
Aude Mariani1, C Jeandel, F Paris
1Service de Pédiatrie 1, Centre Hopitalo-Universitaire Arnaud de Villeneuve, Montpellier, France. a-mariani@chu-montpellier.fr
Insights
Children with idiopathic short stature (ISS) experience delayed puberty and subnormal growth, leading to an unfavorable final height prognosis despite pubertal growth acceleration. Understanding these growth dynamics is key.
Area of Science:
- Pediatric Endocrinology
- Growth and Development
Background:
- Idiopathic short stature (ISS) is associated with an unfavorable prognosis for final height.
- Pubertal growth dynamics significantly influence final height outcomes.
Purpose of the Study:
- To investigate the pubertal growth dynamics in children with idiopathic short stature (ISS).
- To understand how pubertal timing and growth impact final height in ISS.
Main Methods:
- Retrospective cohort study of 50 children diagnosed with ISS.
- Analysis of the pubertal period, including age of onset and peripubertal growth patterns.
Main Results:
- Puberty onset was delayed in children with ISS.
- Prepubertal growth rates were subnormal, with height at -2.45 SD at puberty onset.
- While growth reaccelerated during puberty, it was insufficient to normalize final height.
Conclusions:
- Children with ISS exhibit distinct prepubertal and pubertal growth patterns.
- Significantly delayed puberty contributes to the unfavorable final height prognosis in ISS.
- These growth dynamics offer an explanation for the poor final height outcomes in ISS.
Objective:
As the prognosis for final height is unfavorable for children with idiopathic short stature (ISS), we studied the pubertal growth dynamics in these children, which is a determinant factor in final height.
Subjects/Methods:
In a retrospective cohort study, we analyzed the pubertal period, age of puberty and peripubertal growth in 50 children with ISS.
Results:
The onset of puberty occurred later. Growth rate tended to become increasingly subnormal in the prepubertal period and height was -2.45 SD at puberty onset. Growth reaccelerated at this point, which tended to correct the deviation from the mean height, but it was insufficient to obtain a normal final height.
Conclusions:
The dynamics of growth in children with ISS showed a distinct pattern in the prepubertal and pubertal periods and puberty is significantly delayed in this population. These patterns could explain the unfavorable prognosis for children with ISS.
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