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Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series

Authors

  • Nattaporn Tassanakijpanich Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Hat Yai, ThailandUC Davis MIND Institute, UC Davis Health, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Forrest J McKenzie UC Davis MIND Institute, UC Davis Health, Sacramento, California, USAUniversity of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Yingratana A McLennan UC Davis MIND Institute, UC Davis Health, Sacramento, California, USADepartment of Pediatrics, University of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Elisabeth Makhoul UC Davis MIND Institute, UC Davis Health, Sacramento, California, USADepartment of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Flora Tassone UC Davis MIND Institute, UC Davis Health, Sacramento, California, USADepartment of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Mittal J Jasoliya Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Christopher Romney UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Ignacio Cortina Petrasic UC Davis MIND Institute, UC Davis Health, Sacramento, California, USAUniversity of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Kaye Napalinga UC Davis MIND Institute, UC Davis Health, Sacramento, California, USAMedMom Institute for Human Development, Pasig City, Philippines PubMed articlesGoogle scholar articles
  • Caroline B Buchanan Greenwood Genetic Center, Greenville, South Carolina, USA PubMed articlesGoogle scholar articles
  • Paul Hagerman UC Davis MIND Institute, UC Davis Health, Sacramento, California, USADepartment of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Randi Hagerman UC Davis MIND Institute, UC Davis Health, Sacramento, California, USADepartment of Pediatrics, University of California, Davis, School of Medicine, Sacramento, California, USA PubMed articlesGoogle scholar articles
  • Emily L Casanova Department of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, South Carolina, USA PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Randi Hagerman, UC Davis MIND Institute, UC Davis Health, Sacramento, California 95817, USA; rjhagerman{at}ucdavis.edu
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Citation

Tassanakijpanich N, McKenzie FJ, McLennan YA, et al
Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series

Publication history

  • Received November 21, 2020
  • Accepted June 8, 2021
  • First published June 30, 2021.

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