Literature DB >> 28457480

How should we investigate children with growth failure?

Juliane Léger1.   

Abstract

The early diagnosis of short stature is essential for effective management and treatment. Investigations for children with growth failure are required to distinguish between idiopathic short stature due to physiological variants (familial short stature, and constitutional delays of growth and puberty, or both), primary causes of short stature, such as syndromic and/or genetic defects and skeletal dysplasia, and secondary growth deficits due to endocrine or other chronic disorders such as celiac disease, Crohn's disease, malnutrition, renal, anorexia nervosa or other chronic diseases.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Children; Enfant; Investigations; Petite taille; Short stature; Évaluation

Mesh:

Year:  2017        PMID: 28457480     DOI: 10.1016/j.ando.2017.04.008

Source DB:  PubMed          Journal:  Ann Endocrinol (Paris)        ISSN: 0003-4266            Impact factor:   2.478


  3 in total

1.  Growth impairment and limited range of joint motion in children should raise suspicion of an attenuated form of mucopolysaccharidosis: expert opinion.

Authors:  Nathalie Guffon; Pierre Journeau; Anaïs Brassier; Juliane Leger; Bertrand Chevallier
Journal:  Eur J Pediatr       Date:  2019-02-11       Impact factor: 3.183

2.  Diagnosis of Idiopathic GHD in Children Based on Response to rhGH Treatment: The Importance of GH Provocative Tests and IGF-1.

Authors:  João Soares Felício; Luísa Corrêa Janaú; Marcelle Alves Moraes; Nathalie Abdallah Zahalan; Fabrício de Souza Resende; Manuela Nascimento de Lemos; Norberto Jorge Kzan de Souza Neto; Isabela Imbelloni Farias de Franco; Loyane Tamyres Costa Leitão; Lilian de Souza d'Albuquerque Silva; Maria Clara Neres Iunes de Oliveira; Angélica Leite de Alcântara; Ana Carolina Contente Braga de Souza; Wanderson Maia da Silva; Márcia Costa Dos Santos; Natércia Neves Marques de Queiroz; Lorena Vilhena de Moraes; Antônio Bentes de Figueiredo; Ana Luiza Prieto Farinassi; Luciana Marques da Costa Farias; Danielle Dias da Silva; Karem Miléo Felício; João Felício Abrahão Neto
Journal:  Front Endocrinol (Lausanne)       Date:  2019-09-19       Impact factor: 5.555

3.  Study on pathogenic genes of dwarfism disease by next-generation sequencing.

Authors:  Lv-Lv Yang; Shi-Shan Liang
Journal:  World J Clin Cases       Date:  2021-03-06       Impact factor: 1.337

  3 in total

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