Front. Genet. Frontiers in Genetics Front. Genet. 1664-8021 Frontiers Media S.A. 1143795 10.3389/fgene.2023.1143795 Genetics Correction Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype Doddato et al. 10.3389/fgene.2023.1143795 Doddato Gabriella 1 2 † Fabbiani Alessandra 1 2 3 † Fallerini Chiara 1 2 Bruttini Mirella 1 2 3 Hadjistilianou Theodora 4 Landi Martino 5 Coradeschi Caterina 5 Grosso Salvatore 6 Tomasini Barbara 5 Mencarelli Maria Antonietta 3 Renieri Alessandra 1 2 3 Ariani Francesca 1 2 3 * 1 Medical Genetics, University of Siena, Siena, Tuscany, Italy 2 Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Tuscany, Italy 3 Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy 4 Ophthalmological Science and Neuroscience, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy 5 Terapia Intensiva Neonatale, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy 6 Pediatria, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy

Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland

 *Correspondence: Francesca Ariani, francesca.ariani@unisi.it

These authors have contributed equally to this work and share first authorship

This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Genetics

 25 01 2023 2023 14 1143795 13 01 2023 16 01 2023 Copyright © 2023 Doddato, Fabbiani, Fallerini, Bruttini, Hadjistilianou, Landi, Coradeschi, Grosso, Tomasini, Mencarelli, Renieri and Ariani. 2023 Doddato, Fabbiani, Fallerini, Bruttini, Hadjistilianou, Landi, Coradeschi, Grosso, Tomasini, Mencarelli, Renieri and Ariani

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

 A Corrigendum on Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype by Doddato G, Fabbiani A, Fallerini C, Bruttini M, Hadjistilianou T, Landi M, Coradeschi C, Grosso S, Tomasini B, Mencarelli MA, Renieri A and Ariani F (2021). Front. Genet. 12:761264. doi: 10.3389/fgene.2021.761264 spondyloocular syndrome (SOS) xylosyltransferase II Exome Sequencing (ES) skeletal dysplasia XYLT2

In the published article, there was an error. There was a sentence missing in the Acknowledgments section.

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

“The authors thank the family for participating in the study.”

The corrected sentence appears below:

“The authors thank the family for participating in the study. Two of the authors of this publication are members of the European Reference Network for rare malformation syndromes and rare intellectual and neurodevelopmental disorders, ERN-ITHACA.”

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

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