Symptomatic Hypercalcemia with Vomiting in a Pediatric Patient with Graves' Disease [0.03%]
一名Graves病患儿出现呕吐伴症状性高钙血症病例报告
Goo Lyeon Kim,Kunsong Lee,Ju-Hee Seo et al.
Goo Lyeon Kim et al.
Graves' disease (GD) is the leading cause of childhood hyperthyroidism, resulting from excessive thyroid hormone production. In some cases, it can cause alterations in mineral homeostasis, including calcium, phosphorus, and magnesium, which...
Athanasia Bouliari,Anjile An,Oksana Lekarev et al.
Athanasia Bouliari et al.
Background: Data on the impact of aromatase inhibitor (AI) therapy on final or near-final adult height (FNFH) in males with short stature is limited. This study investigates whether AI therapy improves FNFH in males with ...
Current Approaches and Therapeutic Strategies for Hypothalamic Syndrome in Patients with Childhood-onset Craniopharyngioma [0.03%]
儿童期发病颅咽管瘤患者下丘脑综合征的当前治疗手段和策略
Hermann L Müller
Hermann L Müller
Patients diagnosed with craniopharyngioma often experience rapid and pronounced weight gain that can progress to severe hypothalamic obesity. This phenomenon is predominantly attributed to disruption of critical hypothalamic regulatory circ...
The Relationship Between HbA1c and GMI and Glucose Metrics in Children and Adolescents with Type 1 Diabetes Using AID [0.03%]
CSII与传感器增强泵疗青少年1型糖尿病患者HbA1c和GMI与血糖指标的关系分析
Emrullah Arslan,Hanife Gül Balkı,Deniz Özalp Kızılay et al.
Emrullah Arslan et al.
Introduction: HbA1c remains the standard biomarker for long-term glycemic control, but it lacks precision in capturing short-term glucose variability and acute excursions. This limitation is especially relevant in childre...
The Potential Role of LRG1 in Hepatosteatosis and Insulin Resistance in Obese Children [0.03%]
LRG1在肥胖儿童肝脂变和胰岛素抵抗中潜在作用的探讨
Berna Singin,Zeynep Donbaloğlu,Ebru Barsal Çetiner et al.
Berna Singin et al.
Objective: This study aimed to investigate the relationship between leucine-rich alpha-2-glycoprotein 1 (LRG1), hepatosteatosis, and insulin resistance (IR) in obese children, and to evaluate the potential role of LRG1 as...
Evaluation of Muscle Mass and Strength in Children and Adolescents with Disorders of Sex Development [0.03%]
性发育障碍儿童和青少年的肌肉质量和力量评估
Kürşat Çetin,Zeynep Donbaloğlu,Yasemin Funda Bahar et al.
Kürşat Çetin et al.
Objective: The aim of this study was to evaluate muscle mass and strength in children and adolescents with disorders of sex development (DSD) whose sex assignment was determined by a multidisciplinary team, comparing thes...
Case Reports: Exploring the Varied Presentations and Clinical Features of Carney Complex, A Detailed Report on Three Distinct Cases [0.03%]
病例报告：卡尼综合征的多种表现和临床特征详述三例不同患者病情
İlayda Altun,Hande Turan,Aydilek Dağdeviren et al.
İlayda Altun et al.
Carney Complex (CNC) is a rare genetic disorder characterized by multiple endocrine and nonendocrine neoplasms, primarily driven by mutations in the PRKAR1A gene. This study explores the clinical heterogeneity in CNC patients, with a focus ...
Diagnostic Value of Peak-to-Basal Difference or Ratio of Growth Hormone in Children with Growth Hormone Deficiency [0.03%]
生长激素缺乏症儿童生长激素峰值与基础值差值或比值的诊断价值
Özge Köprülü,Elif Gökçe Basa,İbrahim Mert Erbaş et al.
Özge Köprülü et al.
Introduction: Growth hormone deficiency (GHD) is a rare but important cause of short stature in children. Although GH stimulation tests remain the gold standard for diagnosis, establishing a definitive diagnosis continues...
Osteogenesis Imperfecta with Pes Equinovarus: A Rare Combination and a Rare Col1a1 Variant [0.03%]
成骨不全合并马蹄内翻足一名罕见组合及COL1A1罕见变异病例报告
Nurhan Özcan Murat,Yasemin Alanay
Nurhan Özcan Murat
Variants in the Col1a1 gene typically lead to a connective tissue disorder called osteogenesis imperfecta (OI), which is characterized by increased bone fragility that may be associated with blue sclera, dentinogenesis imperfecta and hearin...
Gender Identity and Preferences in Children with Variations in Sex Development [0.03%]
性发育异常儿童的性别认同及偏好研究进展
Canice E Crerand,Natalie M Gallagher,Margaret P Adam et al.
Canice E Crerand et al.
Objective: To assess gender-typed preferences and gender identity in children with and without variations in sex developments (VSDs). Methods: ...