Research Review of Myhre Syndrome
Maggie R. Brand
Medical Genetics, Department of Pediatrics, Mass General for Children, Boston, Massachusetts, USA
Search for more papers by this authorRyan Monsberger
Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA
Search for more papers by this authorRobert J. Hopkin
Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA
Search for more papers by this authorCorresponding Author
Angela E. Lin
Medical Genetics, Department of Pediatrics, Mass General for Children, Boston, Massachusetts, USA
Correspondence:
Angela E. Lin (lin.angela@mgh.harvard.edu)
Search for more papers by this authorMaggie R. Brand
Medical Genetics, Department of Pediatrics, Mass General for Children, Boston, Massachusetts, USA
Search for more papers by this authorRyan Monsberger
Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA
Search for more papers by this authorRobert J. Hopkin
Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA
Search for more papers by this authorCorresponding Author
Angela E. Lin
Medical Genetics, Department of Pediatrics, Mass General for Children, Boston, Massachusetts, USA
Correspondence:
Angela E. Lin (lin.angela@mgh.harvard.edu)
Search for more papers by this authorAccessibility issue? Request accessibility update.
Funding: The Clinical Research Assistant position for the MGH Myhre Syndrome Clinic is supported in part by the Myhre Syndrome Foundation and generous donors to the MGH Myhre Syndrome Clinic Sundry Fund. Dr. Lin receives support as a consultant to the Myhre Syndrome Foundation.
ABSTRACT
This research review of Myhre syndrome is a summary of published articles which provide a valuable resource for readers, researchers, and future authors. It traces the evolution of the Laryngotracheal–Arthropathy–Prognathism–Short Stature (LAPS) syndrome to the current eponym of Myhre syndrome. These allelic disorders are caused by pathogenic variants in SMAD4. After the initial report over 40 years ago, the steady publication of case reports and small series was accelerated following the discovery of the pathogenic variants in SMAD4. The articles in this review include numerous case reports and small series, reports about basic science, the discovery of the causative gene, the emergence of the natural history in larger studies, and articles about specific features, especially the cardiovascular system and airways. We hope this analysis provides a foundation for future research that may extend symptom-based treatment to genetic-based therapy.
Conflicts of Interest
The authors declare no conflicts of interest.
Data Availability Statement
Data sharing is not applicable to this article as no new data were created or analyzed in this study.
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https://onlinelibrary.wiley.com/doi/10.1002/ajmg.c.32145
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Elkins, L. J., & Spiegelman, M. (2021). pyUserCalc: A revised Jupyter notebook calculator for uranium-series disequilibria in basalts. Earth and Space Science, 8, e2020EA001619. https://doi.org/10.1029/2020EA001619
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