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EDITORIAL article

Front. Pediatr.

Sec. General Pediatrics and Pediatric Emergency Care

This article is part of the Research TopicNovel targets in pediatrics: advances in diagnostic and therapeutic approachesView all 19 articles

"Editorial. Novel targets in pediatrics: advances in diagnostic and therapeutic approaches."

Provisionally accepted
  • 1Azienda Ospedaliera Universitaria Meyer IRCCS - Firenze, Florence, Italy
  • 2Department of Medical and Surgical Sciences (DIMEC), University of Bologna, Italy., Bologna, Italy
  • 3IRCCS Azienda Ospedaliero-Universitaria di Bologna Policlinico di Sant'Orsola, Bologna, Italy
  • 4Immunology Unit, Meyer Children's Hospital IRCCS, Florence, Italy., Firenze, Italy
  • 5Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy., Pavia, Italy
  • 6Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy, Florence, Italy
  • 7Department of Hematology and Oncology, Meyer Children’s Hospital IRCCS, Florence, Italy, Florence, Italy

The final, formatted version of the article will be published soon.

Childhood is a uniquely dynamic and biologically sensitive phase of life during which many diseases-particularly rare, immune-mediated, infectious, and genetically driven conditions-first manifest. Yet, despite this critical window of vulnerability and opportunity, pediatric medicine has historically evolved in the shadow of adult research. Therapeutic strategies are often introduced into pediatric practice only after adult validation, and diagnostic tools are frequently adapted rather than specifically developed for children. Ethical complexities, limited patient numbers, regulatory barriers, and concerns regarding fragility have all contributed to a persistent evidence gap.Consequently, children are frequently exposed to treatments whose age-specific safety, pharmacodynamics, and long-term developmental implications remain incompletely defined.Similarly, diagnostic pathways in pediatrics are often constrained by concerns related to invasiveness, radiation exposure, sedation requirements, and limited pediatric validation studies. However, pediatric medicine is now entering a transformative era. The expansion of targeted therapies, orphan drugs, molecular diagnostics, advanced imaging modalities, bioinformatic platforms, and machinelearning algorithms is redefining what is possible in pediatric care. The 18 contributions included in this Research Topic collectively embody this paradigm shift, spanning rare diseases, infectious and inflammatory conditions, neonatology, critical care, imaging, bioinformatics, digital health, and predictive modeling (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18). Rare diseases remain one of the most compelling frontiers in pediatric medicine. The case report describing infantile fibrosarcoma with a BRAF gene mutation exemplifies the clinical relevance of molecular characterization in rare pediatric tumors. By identifying a non-classical mutation in a gastrointestinal presentation, the study underscores how genomic profiling can refine diagnostic accuracy and inform surgical and oncologic strategies.Equally illustrative is the report on acquired methemoglobinemia in early infancy, a rare but potentially life-threatening condition requiring rapid biochemical confirmation and targeted therapy.Pediatric-onset relapsing polychondritis with airway involvement further reinforces the importance of individualized management strategies in rare inflammatory diseases, integrating surgical innovation with systemic immunomodulation.Other rare or complex presentations discussed in this Topic include acute suppurative appendicitis complicated by gallbladder torsion, highlighting the importance of intraoperative vigilance, and atypical Campylobacter pseudo-appendicitis mimicking surgical abdomen, emphasizing diagnostic refinement to avoid unnecessary procedures. Diagnostic innovation is a recurring theme. The study exploring contrast-enhanced ultrasound in pediatric acute kidney injury provides a radiation-free method to evaluate renal microcirculation and correlate perfusion patterns with pathophysiology (6). Similarly, the randomized controlled trial assessing parental presence during pediatric MRI examinations demonstrates how procedural optimization can reduce sedation requirements and enhance safety.The systematic review and meta-analysis evaluating the predictive value of the direct antiglobulin test for neonatal hyperbilirubinemia critically reassesses a widely used screening tool, advocating for risk-based application rather than routine testing.In infectious diseases, a machine learning-based diagnostic model for severe Mycoplasma pneumoniae pneumonia illustrates how laboratory and clinical markers can be integrated to improve early risk stratification. The application of bioinformatics and transcriptomics is exemplified by the study identifying key genes in pediatric sepsis using weighted gene coexpression network analysis. By distinguishing pediatric-specific molecular signatures from adult datasets, this work reinforces the principle that pediatric immune responses are biologically distinct and require dedicated investigation.Predictive modeling is further advanced by the development of a machine learning-based nomogram for juvenile idiopathic arthritis screening using large national datasets. This tool aims to support early recognition of chronic inflammatory disease in children.Similarly, the predictive model for Henoch-Schönlein purpura nephritis identifies demographic and clinical risk factors associated with renal involvement, offering a structured framework for closer monitoring of high-risk patients. Therapeutic advancement is represented across multiple subspecialties. The systematic review and meta-analysis on neurally adjusted ventilatory assist in pediatric intensive care units evaluates advanced ventilation strategies aimed at optimizing respiratory support and reducing complications.In palliative care, the scoping review on alpha-2 agonists for refractory neurological symptoms explores emerging pharmacologic options for symptom control in children with life-limiting conditions.Emergency medicine is addressed through the systematic review and meta-analysis on migraine treatment in pediatric emergency departments, which synthesizes evidence to support more standardized and effective acute management. Collectively, the 18 articles in this Research Topic provide a cohesive vision of pediatric medicine at a critical juncture. From molecular characterization of rare tumors and immune dysregulation in sepsis, to predictive nomograms for chronic inflammatory diseases, advanced imaging, sedationreduction strategies, digital longitudinal care, and quality-of-life evaluation, the contributions illustrate the convergence of technology, molecular insight, and clinical pragmatism.They affirm that the future of pediatrics lies not in extrapolating adult frameworks but in establishing independent, developmentally informed, and data-driven strategies tailored to children's unique biology and life course. Through sustained innovation, critical appraisal of existing practices (8), and responsible integration of artificial intelligence, pediatric healthcare can progress toward a safer, more precise, and more equitable future for children worldwide.

Keywords: diagnosis, novel aspects, Pediatrics, Rare Diseases, treatments

Received: 03 Feb 2026; Accepted: 16 Feb 2026.

Copyright: © 2026 Catamerò, Conti, Ricci, Votto and Pegoraro. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Francesco Catamerò

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