Paediatrics
Paediatrics

Epidemiology and injury patterns of high-energy pediatric pelvic and acetabular fractures: A retrospective study with comparative outcomes

Ulus Travma Acil Cerrahi Derg. 2026 Sep;32(9):1149-1556. doi: 10.14744/tjtes.2026.00266. ABSTRACT BACKGROUND: This study aimed to evaluate the epidemiological characteristics, injury mechanisms, fracture patterns, associated injuries, …

Residual Disparities in US Adults Hospitalized due to All-Cause Pneumonia Following Implementation of Childhood 13-Valent Pneumococcal Conjugate Vaccine in National Immunization Program

Open Forum Infect Dis. 2026 Aug 24;13(9):ofag528. doi: 10.1093/ofid/ofag528. eCollection 2026 Sep. ABSTRACT BACKGROUND: Use of 13-valent pneumococcal conjugate vaccine (PCV13) has reduced the burden …

Feasibility and Clinical Utility of a Modified Step Test for Evaluating Exercise Intolerance After Pediatric and Adolescent Concussion in the Ambulatory Setting

Sports Health. 2026 Sep 7:19417381261477255. doi: 10.1177/19417381261477255. Online ahead of print. ABSTRACT BACKGROUND: Exercise intolerance (EI) is an important component of concussion pathophysiology, serving as …

Effmann Type IIA2 Urethral Duplication with Anorectal Malformation Complicated by Posterior Urethral Diverticulum: A Staged Minimally Invasive Approach

Surg Case Rep. 2026;12(1):26-0496. doi: 10.70352/scrj.cr.26-0496. Epub 2026 Sep 4. ABSTRACT INTRODUCTION: Urethral duplication associated with anorectal malformation (ARM) is rare and can make both …

Low-dose sulbactam-durlobactam for recurrent CRAB pneumonia in a child with cerebral palsy: a Case Report from a resource-limited setting

Front Pharmacol. 2026 Aug 24;17:1905442. doi: 10.3389/fphar.2026.1905442. eCollection 2026. ABSTRACT BACKGROUND: Pediatric data for sulbactam-durlobactam (SUL-DUR) are extremely scarce, and no standard pediatric dosing exists. …

Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review

Front Genet. 2026 Aug 24;17:1893476. doi: 10.3389/fgene.2026.1893476. eCollection 2026. ABSTRACT INTRODUCTION: Meier-Gorlin syndrome 7 (MGORS7) is a rare autosomal recessive disorder characterized by primordial dwarfism, …