EC Paediatrics

Editorial Volume 15 Issue 1 - 2026

Clinical and Anamnestic Features of the Onset of Reactive Arthritis and Juvenile Idiopathic Arthritis (Ratios for Preliminary Diagnosis)

Ostrovsky IM*, Pshenichnaya EV and Gudenova AS

Federal State Budgetary Educational Institution of Higher Education "Donetsk State Medical University Named After M. Gorky" of the Ministry of Health of the Russian Federation, Russia

*Corresponding Author: Ostrovsky IM, Federal State Budgetary Educational Institution of Higher Education "Donetsk State Medical University Named After M. Gorky" of the Ministry of Health of the Russian Federation, Russia.
Received: December 22, 2025; Published: January 02, 2026



Dilated cardiomyopathy (DCM) in neonates is a rare condition with a broad differential diagnosis, including genetic etiologies. Familial forms of DCM are genetically heterogeneous, recent studies have implicated variants in RPL3L gene, encoding a ribosomal protein, in severe neonatal DCM. We report a case of fulminant heart failure with rapidly progressive neonatal dilated cardiomyopathy and multimodal support, associated with bi-allelic RPL3L variants.

 Keywords: Dilated Cardiomyopathy; RPL3L Gene; Genetic Testing; Neonatal Heart Failure; Heart Transplantation

Ostrovsky IM., et al. “Clinical and Anamnestic Features of the Onset of Reactive Arthritis and Juvenile Idiopathic Arthritis (Ratios for Preliminary Diagnosis)”. EC Paediatrics  15.1 (2026): 01-03.

ECronicon Journal

Our Services

Quick Links

Information

Creative Commons LicenseOpen Access by ECronicon is licensed under a Creative Commons Attribution 4.0 International License
Based on a work at www.ecronicon.net