Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation [0.03%]
甲状腺激素抵抗伴垂体微腺瘤及THRB基因突变一例报告
Jiyeon Kim,Eu Seon Noh,Min-Sun Kim et al.
Jiyeon Kim et al.
Factors affecting bone mineral density in children and adolescents with systemic lupus erythematosus [0.03%]
影响系统性红斑狼疮儿童和青少年骨密度的因素
Su Jin Park,Soo Yeun Sim,Dae Chul Jeong et al.
Su Jin Park et al.
Purpose: Patients with juvenile-onset systemic lupus erythematosus (JSLE) are at a high risk of entering adulthood with disease-related morbidities like reduced bone mass and osteoporosis. This study aimed to evaluate the...
The impacts of COVID-19 on childhood obesity: prevalence, contributing factors, and implications for management [0.03%]
COVID-19对儿童肥胖的影响：流行程度、促成因素及管理意义
Min-Ji Kim,Minji Kim,Ju Young Yoon et al.
Min-Ji Kim et al.
Purpose: This study aimed to identify changes in the prevalence of obesity and related diseases among children and adolescents during the coronavirus disease 2019 (COVID-19) pandemic. ...
Long-term efficacy of a triptorelin 3-month depot in girls with central precocious puberty [0.03%]
促性腺激素释放激素类似物（曲普瑞林）3月剂型治疗中枢性性早熟女孩的长期疗效研究
Kyu Hyun Park,Si-Hwa Gwag,Yu Jin Kim et al.
Kyu Hyun Park et al.
Purpose: Three-month gonadotropin-releasing hormone agonists (GnRHas) are expected to achieve better compliance in patients with central precocious puberty (CPP) compared to the monthly formulation. However, 1-month depot...
Kotb Abbass Metwalley,Hekma Saad Farghaly
Kotb Abbass Metwalley
Idiopathic ketotic hypoglycemia (IKH) is defined as bouts of hypoglycemia with increased blood or urine ketones in certain children after prolonged fasting or during illness. IKH is divided into physiological IKH, which is most frequently o...
Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents [0.03%]
儿童和青少年造血干细胞移植后的长期内分泌后遗症
Soojin Hwang,Yena Lee,Ji-Hee Yoon et al.
Soojin Hwang et al.
Purpose: As the survival rate from pediatric cancers has increased significantly with advances in treatment modalities, long-term endocrine complications have also risen. This study investigated the frequencies and risks ...
Clinical validation of a deep-learning-based bone age software in healthy Korean children [0.03%]
深度学习骨龄软件在健康韩国儿童中临床验证研究
Hyo-Kyoung Nam,Winnah Wu-In Lea,Zepa Yang et al.
Hyo-Kyoung Nam et al.
Purpose: Bone age (BA) is needed to assess developmental status and growth disorders. We evaluated the clinical performance of a deep-learning-based BA software to estimate the chronological age (CA) of healthy Korean chi...
Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effectiveness of gemfibrozil treatment --case report and literature review [0.03%]
六年随访一例家族性乳糜微粒血症综合征患儿：疾病进程和吉非贝齐治疗效果——病例报告及文献复习
Manal Mustafa,Mira Almheiri
Manal Mustafa
Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease affecting lipoprotein metabolism. FCS is estimated to occur in 1 in 1-2 million individuals and can be diagnosed at any age, equally affecting all genders, races,...
Short stature with low serum alkaline phosphatase activity: a case report of hypophosphatasia [0.03%]
低血清碱性磷酸酶活性的矮小身材：低磷骨症的一个病例报告
Donghyun Lee,So Yun Park,Heung Sik Kim et al.
Donghyun Lee et al.
Hypophosphatasia (HPP) is a rare condition characterized by abnormal bone mineralization. The manifestations of HPP vary from no symptoms to intrauterine fetal death; short stature is another indication of HPP. A 3 ½-year-old boy presented...