Rethinking Otorhinolaryngologic Care Pathways in Children with Down Syndrome: A Multidisciplinary Framework for Early Diagnosis and Management [0.03%]
重新思考唐氏综合症儿童耳鼻喉护理路径：早期诊断和管理的多学科框架
Francesco Fabrizio Comisi,Elena Esposito,Salvatore Savasta
Francesco Fabrizio Comisi
Background: Children with Down syndrome (DS) are at high risk for a broad spectrum of otorhinolaryngologic (ENT) disorders, including hearing impairment, obstructive sleep apnea (OSA), dysphagia, and language delay. These conditions often c...
White matter trajectories in Down syndrome and Alzheimer's disease: Insights from diffusion tensor-based morphometry [0.03%]
Down综合征和阿尔茨海默病的白质纤维轨迹：基于扩散张量的形态计量学研究见解
Fedal Saini,Phoebe Ivain,Mina Idris et al.
Fedal Saini et al.
Introduction: Diffusion magnetic resonance imaging studies investigating Down syndrome (DS) and Alzheimer's disease (AD) have mainly relied on white matter (WM) skeleton-based techniques, potentially overlooking broader W...
Permanent dental development radiographically assessed in children and adolescents with down syndrome - systematic review and meta-analysis [0.03%]
儿童和青少年唐氏综合征患者永久性牙齿发育的放射学评估-系统回顾和荟萃分析
Maria Isabel Gomes França,Debora Duarte Moreira,Carolina Lima Lopes et al.
Maria Isabel Gomes França et al.
Objective: To systematically revisit the existing scientific literature and investigate whether Down syndrome can affect the chronology of dental development in children and adolescents. ...
Nutritional status, dental caries and parental attitude to junior oral hygiene among children and adolescents with Down syndrome [0.03%]
唐氏综合症儿童和青少年的营养状况、龋齿和父母对口腔卫生的态度
Ramah Eimad Makieh,Chaza Nader Kouchaji
Ramah Eimad Makieh
Background: Children with Down syndrome (DS) frequently experience nutritional issues. Some of them are attributed to gastrointestinal tract abnormalities, while others are due to feeding behaviors. Previous studies have ...
Deciphering Haploid Chromosome Conformation Alternation in Down Syndrome by Multiple Haploid Omics Analysis [0.03%]
利用单倍体组学分析解码唐氏综合症中的单倍体染色体构象变化
Chengchao Wu,Tianshu Zhou,Wenfu Ke et al.
Chengchao Wu et al.
For chromosome abnormalities (CA), such as Down syndrome (DS), the influence of genomic variations to chromosome conformation and gene transcription remains elusive. Based on the complete genomic sequence from the parents of the DS trisomy ...
Lauren N Dunn,Brian F Niemeyer,Neetha P Eduthan et al.
Lauren N Dunn et al.
Trisomy 21 (T21) gives rise to Down syndrome (DS), the most commonly occurring chromosomal abnormality in humans. T21 affects nearly every organ and tissue system in the body, predisposing individuals with DS to congenital heart defects, au...
Mechanistic insights into Down syndrome comorbidities via convergent RNA-seq and TWAS signals [0.03%]
通过聚合RNA测序和TWAS信号洞察唐氏综合症并发疾病的作用机制
Marc Subirana-Granés,Haoyu Zhang,Prashant Gupta et al.
Marc Subirana-Granés et al.
Down syndrome (DS) is caused by trisomy of chromosome 21 and is associated with diverse clinical manifestations, yet the molecular pathways linking chromosome-21 dosage effects to DS comorbidities remain poorly defined. Here we address this...
Disease-specific neuropathological alterations of the locus coeruleus in Alzheimer's disease, Down syndrome, and Parkinson's disease [0.03%]
阿尔茨海默病、唐氏综合征和帕金森病中蓝斑的疾病特异性神经病理变化
Marta Fructuoso,Yannick Vermeiren,Susana Boluda et al.
Marta Fructuoso et al.
Introduction: The locus coeruleus (LC), the brain's primary source of noradrenaline (NA), undergoes early neurodegeneration in Parkinson's disease (PD), Alzheimer's diseases (AD), and Down syndrome (DS); however, differen...
Hidradenitis suppurativa in pediatric patients with Down Syndrome: a comparative study of 116 cases and controls [0.03%]
Down综合征患儿脓疱性汗腺炎的病例对照研究
Maria Sin-Soler,Magdalini Louka,Patricia Garbayo-Salmons et al.
Maria Sin-Soler et al.
Background: Hidradenitis suppurativa (HS) seems to be more prevalent in patients with Down syndrome (DS), with earlier onset, higher incidence in females, and increased body mass index (BMI) in these individuals. ...
"Bubbly heart," a case report of Morgagni hernia delayed diagnosis in patient with Down syndrome: The hernia is in the details [0.03%]
“ bubbly heart ” —易患唐氏综合症患者的 Morgagni 隔疝延迟诊断病例报告：疝气就在细节之中
Valerio D&#x;Agostino,Giulia Valente,Emanuela Federico et al.
Valerio D&#x;Agostino et al.
Morgagni hernia represents a rare form of congenital diaphragmatic hernia (2%-5%), characterized by a defect in the anterior and retrosternal diaphragm. It can be associated with other congenital anomalies, especially in conditions like Dow...
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