指南
基因检测
医学
身材矮小
特发性矮身高
病因学
遗传诊断
遗传咨询
家族史
儿科
梅德林
临床实习
遗传倾向
重症监护医学
医学检查
生物信息学
家庭医学
遗传综合征
作者
Andrew Dauber,Alexander A L Jorge,O. Nilsson,Olaf M Dekkers,Jesús Argente,Irène Netchine,Philippe Backeljauw,Jeffrey Baron,Débora Romeo Bertola,Peter Clayton,Justin H Davies,Thomas Edouard,Thomas Eggermann,Evelien F Pease Gevers,Giedré Grigelioniené,Karen E. Heath,Youn Hee Jee,Pablo Lapunzina,Geert Mortier,Stepanka Pruhova
标识
DOI:10.1093/ejendo/lvag013
摘要
Short stature may be caused by a multitude of conditions, including genetic and non-genetic causes. Over the last decade, advances in genetic sequencing technologies have revolutionized our understanding of the underlying physiology of growth and greatly increased our ability to identify genetic etiologies of short stature. The current guideline provides a general overview of the approach to the evaluation of a child with short stature, followed by recommendations identifying factors in the medical and family history, physical examination, radiographic, and laboratory work up which increase the likelihood of identifying a genetic etiology. An algorithm is proposed for the genetic workup of individuals with short stature based on their clinical presentation. The benefits and risks of genetic testing are discussed as well.
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