Severe Neonatal Episodic Laryngospasm (SNEL) due to Mutation in the SCN4A Gene as a Rare Differential Diagnosis in Paroxysmal Inspiratory Stridor with Cyanosis in Infancy
Klin Padiatr
.
2024 Oct 28.
doi: 10.1055/a-2423-8849.
Online ahead of print.
Authors
Julia Westhoff
1
,
Rahel Schuler
2
,
Lutz Nährlich
1
,
Andreas Hahn
3
Affiliations
1
Department of Pediatrics, Pediatric Pneumology, Justus-Liebig-Universität Giessen, Giessen, Germany.
2
Department of Pediatrics, Neonatology, Justus-Liebig-Universitat Giessen, Giessen, Germany.
3
Department of Pediatrics, Child Neurology, Justus-Liebig-Universität Giessen, Giessen, Germany.
PMID:
39467576
DOI:
10.1055/a-2423-8849
No abstract available