Deciphering short stature in children

Bibliographic Details
Title: Deciphering short stature in children
Authors: Nella Polidori, Valeria Castorani, Angelika Mohn, Francesco Chiarelli
Source: Annals of Pediatric Endocrinology & Metabolism, Vol 25, Iss 2, Pp 69-79 (2020)
Publisher Information: Korean Society of Pediatric Endocrinology, 2020.
Publication Year: 2020
Collection: LCC:Pediatrics
Subject Terms: growth, short stature, child, height, anthropometric measurements, auxology, growth hormone therapy, Pediatrics, RJ1-570
More Details: Short stature is a common reason for referral to pediatric endocrinologists. Multiple factors, including genetic, prenatal, postnatal, and local environmental factors, can impair growth. The majority of children with short stature, which can be defined as a height less than 2 standard deviation score below the mean, are healthy. However, in some cases, they may have an underlying relevant disease; thus, the aim of clinical evaluation is to identify the subset of children with pathologic conditions, for example growth hormone deficiency or other hormonal abnormalities, Turner syndrome, inflammatory bowel disease, or celiac disease. Prompt identification and management of these children can prevent excessive short stature in adulthood. In addition, a thorough clinical assessment may allow evaluation of the severity of short stature and likely growth trajectory to identify the most effective interventions. Consequently, appropriate diagnosis of short stature should be performed as early as possible and personalized treatment should be started in a timely manner. An increase in knowledge and widespread availability of genetic and epigenetic testing in clinical practice in recent years has empowered the diagnostic process and appropriate treatment for short stature. Furthermore, novel treatment approaches that can be used both as diagnostic tools and as therapeutic agents have been developed. This article reviews the diagnostic approach to children with short stature, discusses the main causes of short stature in children, and reports current therapeutic approaches and possible future treatments.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2287-1012
2287-1292
Relation: http://e-apem.org/upload/pdf/apem-2040064-032.pdf; https://doaj.org/toc/2287-1012; https://doaj.org/toc/2287-1292
DOI: 10.6065/apem.2040064.032
Access URL: https://doaj.org/article/bffc926042ce4354a301f5de247619db
Accession Number: edsdoj.bffc926042ce4354a301f5de247619db
Database: Directory of Open Access Journals
More Details
ISSN:22871012
22871292
DOI:10.6065/apem.2040064.032
Published in:Annals of Pediatric Endocrinology & Metabolism
Language:English