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An approach to constitutional delay of growth and puberty

Constitutional delay of growth and puberty is a transient state of hypogonadotropic hypogonadism associated with prolongation of childhood phase of growth, delayed skeletal maturation, delayed and attenuated pubertal growth spurt, and relatively low insulin-like growth factor-1 secretion. In a consi...

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Detalles Bibliográficos
Autores principales: Soliman, Ashraf T., Sanctis, Vincenzo De
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475892/
https://www.ncbi.nlm.nih.gov/pubmed/23087852
http://dx.doi.org/10.4103/2230-8210.100650
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author Soliman, Ashraf T.
Sanctis, Vincenzo De
author_facet Soliman, Ashraf T.
Sanctis, Vincenzo De
author_sort Soliman, Ashraf T.
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description Constitutional delay of growth and puberty is a transient state of hypogonadotropic hypogonadism associated with prolongation of childhood phase of growth, delayed skeletal maturation, delayed and attenuated pubertal growth spurt, and relatively low insulin-like growth factor-1 secretion. In a considerable number of cases, the final adult height (Ht) does not reach the mid-parental or the predicted adult Ht for the individual, with some degree of disproportionately short trunk. In the pre-pubertal male, testosterone (T) replacement therapy can be used to induce pubertal development, accelerate growth and relieve the psychosocial complaints of the adolescents. However, some issues in the management are still unresolved. These include type, optimal timing, dose and duration of sex steroid treatment and the possible use of adjunctive or alternate therapy including: oxandrolone, aromatase inhibitors and human growth hormone.
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spelling pubmed-34758922012-10-19 An approach to constitutional delay of growth and puberty Soliman, Ashraf T. Sanctis, Vincenzo De Indian J Endocrinol Metab Review Article Constitutional delay of growth and puberty is a transient state of hypogonadotropic hypogonadism associated with prolongation of childhood phase of growth, delayed skeletal maturation, delayed and attenuated pubertal growth spurt, and relatively low insulin-like growth factor-1 secretion. In a considerable number of cases, the final adult height (Ht) does not reach the mid-parental or the predicted adult Ht for the individual, with some degree of disproportionately short trunk. In the pre-pubertal male, testosterone (T) replacement therapy can be used to induce pubertal development, accelerate growth and relieve the psychosocial complaints of the adolescents. However, some issues in the management are still unresolved. These include type, optimal timing, dose and duration of sex steroid treatment and the possible use of adjunctive or alternate therapy including: oxandrolone, aromatase inhibitors and human growth hormone. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3475892/ /pubmed/23087852 http://dx.doi.org/10.4103/2230-8210.100650 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Soliman, Ashraf T.
Sanctis, Vincenzo De
An approach to constitutional delay of growth and puberty
title An approach to constitutional delay of growth and puberty
title_full An approach to constitutional delay of growth and puberty
title_fullStr An approach to constitutional delay of growth and puberty
title_full_unstemmed An approach to constitutional delay of growth and puberty
title_short An approach to constitutional delay of growth and puberty
title_sort approach to constitutional delay of growth and puberty
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475892/
https://www.ncbi.nlm.nih.gov/pubmed/23087852
http://dx.doi.org/10.4103/2230-8210.100650
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