The Etiological Spectrum of Short Stature among Children Attending Endocrine Clinic at Tertiary Care Hospital

{"title":"The Etiological Spectrum of Short Stature among Children Attending Endocrine Clinic at Tertiary Care Hospital","authors":"","doi":"10.37184/lnjpc.2707-3521.6.8","DOIUrl":null,"url":null,"abstract":"Background: One of the most frequent reasons for referral to pediatric endocrinology units is short stature. Children's short height has a complicated etiology that includes genetics, race, gender, nutrition, and several endocrine hormones.\n\nObjective: To determine the etiological spectrum of short stature among children presenting to endocrinology outpatient clinics in a tertiary care hospital.\n\nMethods: This descriptive cross-sectional study was performed in the outpatient clinic of the Endocrinology Department at the National Institute of Child Health Hospital from September to December 2022. Short stature was defined as height for age <-2 standard deviations for the corresponding age and gender according to World Health Organization growth charts. 263 children were enrolled in the study. Detailed history and panel investigation for short stature were mediated for each child.\n\nResults: A total of 263 patients were enrolled in the study having a median age of 8 (IQR=6-9) years and the majority were females (53.2%). The median SD of height and current weight was -3.48 (IQR= -4.3 - -2.83) and -2.8 (IQR= -3.59 - -2.17) respectively. The most frequently seen classification of short stature was the normal variant (68.1%) followed by endocrine disorders (19.8%), dysmorphic syndrome (9.9%), and chronic disease (2.3%). The most common cause of short stature was familial short stature (47.9%) followed by growth hormone deficiency (18.3%), constitutional short stature (9.1%), Turner syndrome (9.1%), both familial and constitutional SS (8%), idiopathic short stature (3%), celiac disease (2.3%), Cushing syndrome (n=2, 0.8%), panhypopituitarism (0.8%) and Seckel syndrome (0.8%).\n\nConclusion: This study analyzed that the majority of short stature are normal variants. However, findings of endocrine disorders, dysmorphic disorders, and chronic disease suggest timely screening and detection of short stature to avoid serious consequences of silent underlying diseases.","PeriodicalId":140679,"journal":{"name":"Liaquat National Journal of Primary Care","volume":"27 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Liaquat National Journal of Primary Care","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37184/lnjpc.2707-3521.6.8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: One of the most frequent reasons for referral to pediatric endocrinology units is short stature. Children's short height has a complicated etiology that includes genetics, race, gender, nutrition, and several endocrine hormones. Objective: To determine the etiological spectrum of short stature among children presenting to endocrinology outpatient clinics in a tertiary care hospital. Methods: This descriptive cross-sectional study was performed in the outpatient clinic of the Endocrinology Department at the National Institute of Child Health Hospital from September to December 2022. Short stature was defined as height for age <-2 standard deviations for the corresponding age and gender according to World Health Organization growth charts. 263 children were enrolled in the study. Detailed history and panel investigation for short stature were mediated for each child. Results: A total of 263 patients were enrolled in the study having a median age of 8 (IQR=6-9) years and the majority were females (53.2%). The median SD of height and current weight was -3.48 (IQR= -4.3 - -2.83) and -2.8 (IQR= -3.59 - -2.17) respectively. The most frequently seen classification of short stature was the normal variant (68.1%) followed by endocrine disorders (19.8%), dysmorphic syndrome (9.9%), and chronic disease (2.3%). The most common cause of short stature was familial short stature (47.9%) followed by growth hormone deficiency (18.3%), constitutional short stature (9.1%), Turner syndrome (9.1%), both familial and constitutional SS (8%), idiopathic short stature (3%), celiac disease (2.3%), Cushing syndrome (n=2, 0.8%), panhypopituitarism (0.8%) and Seckel syndrome (0.8%). Conclusion: This study analyzed that the majority of short stature are normal variants. However, findings of endocrine disorders, dysmorphic disorders, and chronic disease suggest timely screening and detection of short stature to avoid serious consequences of silent underlying diseases.
三级医院内分泌门诊儿童身材矮小的病因谱分析
背景:转诊到儿科内分泌科最常见的原因之一是身材矮小。儿童身高不足的病因复杂,包括遗传、种族、性别、营养和几种内分泌激素。目的:了解某三级医院内分泌科门诊儿童矮小的病因谱。方法:本描述性横断面研究于2022年9月至12月在国立儿童保健医院内分泌科门诊进行。根据世界卫生组织的生长图表,身高不足被定义为年龄小于相应年龄和性别的2个标准差。263名儿童参加了这项研究。对每个儿童进行详细的病史和矮小的小组调查。结果:共纳入263例患者,中位年龄为8岁(IQR=6-9)岁,以女性为主(53.2%)。身高和体重的SD中位数分别为-3.48 (IQR= -4.3 - -2.83)和-2.8 (IQR= -3.59 - -2.17)。身材矮小最常见的分类是正常变异(68.1%),其次是内分泌失调(19.8%)、畸形综合征(9.9%)和慢性病(2.3%)。最常见的矮小原因是家族性矮小(47.9%),其次是生长激素缺乏症(18.3%)、体质矮小(9.1%)、特纳综合征(9.1%)、家族性和体质性SS(8%)、特发性矮小(3%)、乳糜泻(2.3%)、库欣综合征(n=2, 0.8%)、全垂体功能低下(0.8%)和塞克尔综合征(0.8%)。结论:本研究分析了大多数矮个子是正常变异。然而,内分泌失调、畸形障碍和慢性疾病的发现建议及时筛查和发现身材矮小,以避免隐匿的潜在疾病的严重后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信