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...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
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Frontiers Media S.A.
2026-01-01
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| Cyfres: | Frontiers in Pediatrics |
| Pynciau: | |
| Mynediad Ar-lein: | https://www.frontiersin.org/articles/10.3389/fped.2025.1648611/full |
| Tagiau: |
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