Paediatrics
Paediatrics

Prevalence and duration of clinical symptoms of pediatric long COVID: findings from a one-year prospective study

Front Pediatr. 2025 Sep 22;13:1645228. doi: 10.3389/fped.2025.1645228. eCollection 2025. ABSTRACT BACKGROUND: Long COVID in children remains a poorly understood condition with wide variability in clinical …

Case Report: Clinical case analysis of gaucher disease management in a resource-limited setting: a single center experience from Kashigar, Xinjiang Uygur Autonomous Region, the Western China

Front Pediatr. 2025 Sep 22;13:1530177. doi: 10.3389/fped.2025.1530177. eCollection 2025. ABSTRACT OBJECTIVE: This report presents the inaugural case of Gaucher disease identified in Kashgar Prefecture, Xinjiang, …

Exome Sequencing Analysis and Clinical Features of a Chinese Patient with 3M Syndrome and A Review of Literature

Appl Clin Genet. 2025 Oct 2;18:189-197. doi: 10.2147/TACG.S538739. eCollection 2025. ABSTRACT BACKGROUND: 3M syndrome is a rare autosomal recessive genetic disorder characterized by significant intrauterine …

Currently managed US prevalence of cutaneous venous malformations (cVMs): a nationally representative, retrospective, real-world, subject-blinded, physician-observational probability study

Orphanet J Rare Dis. 2025 Oct 7;20(1):504. doi: 10.1186/s13023-025-03995-8. ABSTRACT BACKGROUND: Cutaneous venous malformations (cVMs) are rare vascular anomalies characterized by progressive vessel ectasia, leading …

Development and external validation of a machine learning-based predictive model for acute kidney injury in hospitalized children with idiopathic nephrotic syndrome

BMC Med Inform Decis Mak. 2025 Oct 7;25(1):364. doi: 10.1186/s12911-025-03203-4. NO ABSTRACT PMID:41057927 | DOI:10.1186/s12911-025-03203-4

X-linked hypophosphatemia and tumor-induced osteomalacia: a narrative review and expert opinion on the diagnostic and therapeutic challenges in the era of burosumab

Orphanet J Rare Dis. 2025 Oct 7;20(1):505. doi: 10.1186/s13023-025-03952-5. NO ABSTRACT PMID:41057893 | DOI:10.1186/s13023-025-03952-5