Front. Pediatr. Frontiers in Pediatrics Front. Pediatr. 2296-2360 Frontiers Media S.A. 10.3389/fped.2025.1651138 Pediatrics Correction Correction: Case Report: Diagnosis of Gaucher disease in a toddler with acute respiratory failure HouseholderSarah 1 2 † NagarRuchit 1 2 † ShahNisarg 3 ForwardJodi 4 BickertonSean 1 MistryPramod 5 FaustinoE. Vincent S. 6 * Department of Pediatrics, Yale-New Haven Hospital, New Haven, CT, United States Department of Internal Medicine, Yale-New Haven Hospital, New Haven, CT, United States Yale School of Medicine, New Haven, CT, United States Secion of Hematology/Oncology, Department of Pediatrics, Yale-New Haven Hospital, New Haven, CT, United States Section of Digestive Diseases, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, United States Section of Critical Care, Department of Pediatrics, Yale School of Medicine, New Haven, CT, United States

Edited and Reviewed by: Cinzia Ciccacci, Saint Camillus International University of Health and Medical Sciences, Italy

 Correspondence: E. Vincent S. Faustino vince.faustino@yale.edu

These authors share first authorship

 12082025 2025 131651138 20062025 14072025 © 2025 Householder, Nagar, Shah, Forward, Bickerton, Mistry and Faustino. 2025Householder, Nagar, Shah, Forward, Bickerton, Mistry and Faustino

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 A Correction on Case report: diagnosis of Gaucher disease in a toddler with acute respiratory failure By Householder S, Nagar R, Shah N, Forward J, Bickerton S, Mistry P and Faustino EVS (2025). Front. Pediatr. 13:1476541. doi: 10.3389/fped.2025.1476541 Gaucher disease stridor pediatric ARDS gene replacement therapy case report section-at-acceptanceGenetics of Common and Rare Diseases

In the published article, there was an error. We refer to a specific gene mutation as “p.L484P”. However the correct gene is actually “p.L483P”.

A correction has been made to the Abstract. This sentence previously stated:

“Rapid whole genome sequence showed a compound heterozygote mutation in the GBA1 gene involving a maternally inherited known pathogenic variant, p.L484P, and a paternally inherited novel likely pathogenic variant, p.P358l.”

The corrected sentence appears below:

“Rapid whole genome sequence showed a compound heterozygote mutation in the GBA1 gene involving a maternally inherited known pathogenic variant, p.L483P, and a paternally inherited novel likely pathogenic variant, p.P358l.”

A correction has also been made to Case Presentation, Paragraph 6. This sentence previously stated:

“One variant (p.L484P) was an established disease mutation associated with neuronal subtype of Gaucher disease when present in homozygous state.”

The corrected sentence appears below:

“One variant (p.L483P) was an established disease mutation associated with neuronal subtype of Gaucher disease when present in homozygous state.”

The original article has been updated.

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