Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations

Eva Vanbelleghem^#^{1

2}, Tim Van Damme^#¹, Aude Beyens^{1

2}, Sofie Symoens^{1

2}, Kathleen Claes^{1

2}, Julie De Backer^{1

3}, Ilse Meerschaut⁴, Floris Vanommeslaeghe⁵, Sigurd E Delanghe⁵, Jenneke van den Ende⁶, Tessi Beyltjens⁶, Eleanor R Scimone⁷, Mark E Lindsay^{8

9}, Lisa A Schimmenti¹⁰, Alicia M Hinze¹¹, Emily Dunn¹², Natalia Gomez-Ospina¹², Isabelle Vandernoot¹³, Thomas Delguste¹³, Sandra Coppens¹³, Valérie Cormier-Daire¹⁴, Marco Tartaglia¹⁵, Livia Garavelli¹⁶, Joseph Shieh¹⁷, Şenol Demir¹⁸, Esra Arslan Ateş¹⁹, Martin Zenker²⁰, Mersedeh Rohanizadegan²¹, Greysha Rivera-Cruz²², Sofia Douzgou²³; Myhre Syndrome Foundation; Angela E Lin⁷, Bert Callewaert^{24

25}

Collaborators, Affiliations

Collaborators

Myhre Syndrome Foundation:
Justin Smith, Jessica Simkins, Don Clark, Stephanie Karatsinides, Sandy Taylor, Ines White, Patti Schultz, Kate Wears, Levi Holder, Kathy Young

Affiliations

¹ Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
² Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
³ Department of Cardiology, Ghent University Hospital, Ghent, Belgium.
⁴ Department of Pediatric Cardiology, University Hospital Brussels, Brussels, Belgium.
⁵ Department of Nephrology, Ghent University Hospital, Ghent, Belgium.
⁶ Department of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.
⁷ Department of Pediatrics, Genetics Unit, MassGeneral for Children, Boston, MA, USA.
⁸ Cardiovascular Genetics Program, Cardiology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
⁹ Pediatric Cardiology Division, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA.
¹⁰ Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
¹¹ Division of Rheumatology, Mayo Clinic, Rochester, MN, USA.
¹² Department of Pediatrics, Division of Medical Genetic, Stanford University, Stanford, CA, USA.
¹³ ULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
¹⁴ Paris Cité University, Centre of Reference for Constitutional Bone Diseases (MOC), Department of Genetics, INSERM UMR 1163, Imagine Institute, Necker-Enfants Malades Hospital, Paris, France.
¹⁵ Molecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
¹⁶ Medical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
¹⁷ Institute for Human Genetics and Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.
¹⁸ Department of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.
¹⁹ Department of Medical Genetics, Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.
²⁰ Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
²¹ Department of Medicine, Division of Translational Medicine & Human Genetics, University of Pennsylvania, Philadelphia, PA, USA.
²² Division of Reproductive Endocrinology and Infertility, Stanford University School of Medicine, Stanford, CA, USA.
²³ Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
²⁴ Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium. bert.callewaert@ugent.be.
²⁵ Department of Biomolecular Medicine, Ghent University, Ghent, Belgium. bert.callewaert@ugent.be.

^# Contributed equally.

PMID: 39256535
DOI: 10.1038/s41431-024-01690-z

Published Erratum

Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations

Eva Vanbelleghem et al. Eur J Hum Genet. 2024.

. 2024 Sep 10.

doi: 10.1038/s41431-024-01690-z. Online ahead of print.

Authors

Collaborators

Myhre Syndrome Foundation:
Justin Smith, Jessica Simkins, Don Clark, Stephanie Karatsinides, Sandy Taylor, Ines White, Patti Schultz, Kate Wears, Levi Holder, Kathy Young

Affiliations

¹ Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
² Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
³ Department of Cardiology, Ghent University Hospital, Ghent, Belgium.
⁴ Department of Pediatric Cardiology, University Hospital Brussels, Brussels, Belgium.
⁵ Department of Nephrology, Ghent University Hospital, Ghent, Belgium.
⁶ Department of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.
⁷ Department of Pediatrics, Genetics Unit, MassGeneral for Children, Boston, MA, USA.
⁸ Cardiovascular Genetics Program, Cardiology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
⁹ Pediatric Cardiology Division, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA.
¹⁰ Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
¹¹ Division of Rheumatology, Mayo Clinic, Rochester, MN, USA.
¹² Department of Pediatrics, Division of Medical Genetic, Stanford University, Stanford, CA, USA.
¹³ ULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
¹⁴ Paris Cité University, Centre of Reference for Constitutional Bone Diseases (MOC), Department of Genetics, INSERM UMR 1163, Imagine Institute, Necker-Enfants Malades Hospital, Paris, France.
¹⁵ Molecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
¹⁶ Medical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
¹⁷ Institute for Human Genetics and Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.
¹⁸ Department of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.
¹⁹ Department of Medical Genetics, Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.
²⁰ Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
²¹ Department of Medicine, Division of Translational Medicine & Human Genetics, University of Pennsylvania, Philadelphia, PA, USA.
²² Division of Reproductive Endocrinology and Infertility, Stanford University School of Medicine, Stanford, CA, USA.
²³ Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
²⁴ Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium. bert.callewaert@ugent.be.
²⁵ Department of Biomolecular Medicine, Ghent University, Ghent, Belgium. bert.callewaert@ugent.be.

^# Contributed equally.

PMID: 39256535
DOI: 10.1038/s41431-024-01690-z

No abstract available

PubMed Disclaimer

Erratum for

Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.
Vanbelleghem E, Van Damme T, Beyens A, Symoens S, Claes K, De Backer J, Meerschaut I, Vanommeslaeghe F, Delanghe SE, van den Ende J, Beyltjens T, Scimone ER, Lindsay ME, Schimmenti LA, Hinze AM, Dunn E, Gomez-Ospina N, Vandernoot I, Delguste T, Coppens S, Cormier-Daire V, Tartaglia M, Garavelli L, Shieh J, Demir Ş, Arslan Ateş E, Zenker M, Rohanizadegan M, Rivera-Cruz G, Douzgou S; Myhre Syndrome Foundation; Lin AE, Callewaert B. Vanbelleghem E, et al. Eur J Hum Genet. 2024 Sep;32(9):1086-1094. doi: 10.1038/s41431-024-01664-1. Epub 2024 Jul 12. Eur J Hum Genet. 2024. PMID: 38997468 Free PMC article.

Publication types

Actions

LinkOut - more resources

Full Text Sources
- Nature Publishing Group

Save citation to file

Email citation

Add to Collections

Add to My Bibliography

Your saved search

Create a file for external citation management software

Your RSS Feed

Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations

Collaborators

Affiliations

Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations

Authors

Collaborators

Affiliations

Erratum for

Publication types

LinkOut - more resources

Full Text Sources