Neonatal congenital myotonic dystrophy with DMPK gene expansion: clinical features and short-term outcomes

ObjectiveTo investigate the clinical manifestations, diagnosis and treatment, and DMPK gene mutations in neonates with congenital myotonic dystrophy (CDM).MethodsA retrospective analysis was conducted on the clinical data of four neonates diagnosed with CDM and admitted to the Department of Neonatol...

Ausführliche Beschreibung

Bibliografische Detailangaben

Hauptverfasser:	Qian Zhao, Shupeng Wang, Yang Wang, Shenggang Ding
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Frontiers Media S.A. 2026-01-01
Schriftenreihe:	Frontiers in Pediatrics
Schlagworte:	congenital myotonic dystrophy DMPK gene neonatal hypotonia polyhydramnios respiratory failure
Online-Zugang:	https://www.frontiersin.org/articles/10.3389/fped.2025.1648611/full
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