Essaddam Leïla, Kallali Wafa, Cherifi Emna, Guedri Rahma, Mattoussi Nadia, Fitouri Zohra, Ben Becher Saayda
Université de Tunis El Manar, Faculté de Médecine de Tunis, 1007, Tunis, Tunisia.
Children Hospital Béchir Hamza de Tunis, Jebbari, 1007, Tunis, Tunisia.
Int J Pediatr Adolesc Med. 2020 Jun;7(2):74-77. doi: 10.1016/j.ijpam.2019.07.005. Epub 2019 Jul 4.
Short stature is a common reason for referral to pediatric endocrinology clinics. It may be a manifestation of a pathological condition requiring early treatment. The aim of this study was to describe the characteristics and etiologies of short stature among children referred to the pediatric endocrinology clinic of the main pediatric tertiary care center in Tunisia.
Retrospective and descriptive study in the endocrinology unit of children referred for short stature between January 2012 and December 2016. Data on the patients' medical history, physical findings, laboratory tests, bone age and chromosomal analysis were collected.
470 children (266 males and 204 females) were referred during that period. 214 (45.5%) had normal height, and 80.8% of them were referred by general practitioners. The other 256 children (54.5%) had a confirmed short stature (mean age :7.2 years, mean height: -2.77 SDS). Endocrinological causes were the most common(43% GHD, 4% hypothyroidism) followed by intrauterine growth retardation IUGR (24%), genetic syndromes (8.4%), chronic pediatric diseases (7.8%), skeletal dysplasia (6.2%), normal variant of short stature (5%), and psychosocial deprivation (1.2%). Among non-endocrine causes, Turner syndrome was the most common genetic syndrome (4.4%), achondroplasia the main skeletal dysplasia (4%) and celiac disease the main chronic disease (3.4%).
ST is largely overestimated in our country. Therefore, it is important to insist on adequate measurement and analysis of growth parameters to avoid unnecessary investigations. GHD and IUGR were the most common causes. Celiac disease, though frequent in Tunisia, is not a common cause of short stature.
身材矮小是转诊至儿科内分泌诊所的常见原因。它可能是需要早期治疗的病理状况的一种表现。本研究的目的是描述转诊至突尼斯主要儿科三级护理中心儿科内分泌诊所的儿童身材矮小的特征和病因。
对2012年1月至2016年12月因身材矮小转诊的儿童内分泌科进行回顾性描述性研究。收集患者的病史、体格检查结果、实验室检查、骨龄和染色体分析数据。
在此期间转诊了470名儿童(266名男性和204名女性)。214名(45.5%)身高正常,其中80.8%由全科医生转诊。其他256名儿童(54.5%)确诊身材矮小(平均年龄:7.2岁,平均身高:-2.77 SDS)。内分泌原因最为常见(43%生长激素缺乏症,4%甲状腺功能减退症),其次是宫内生长迟缓(IUGR)(24%)、遗传综合征(8.4%)、儿童慢性疾病(7.8%)、骨骼发育不良(6.2%)、身材矮小正常变异型(5%)和心理社会剥夺(1.2%)。在非内分泌原因中,特纳综合征是最常见的遗传综合征(4.4%),软骨发育不全是主要的骨骼发育不良(4%),乳糜泻是主要的慢性疾病(