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Phenotypes
Original research
Arterial aneurysm and dissection: toward the evolving phenotype of Tatton-Brown-Rahman syndrome

Authors

  • Vicken Totten Kaweah Health System, Visalia, California, USA Kayenta Health Center of the Indian Health Service, Kayenta, Arizona, USA PubMed articlesGoogle scholar articles
  • Gisela Teixido-Tura Department of Cardiology, Hospital Universitari Vall d'Hebron, CIBER-CV, Vall d'Hebron institut de Recerca, Universitat Autònoma de Barcelona, Barcelona, Spain Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain PubMed articlesGoogle scholar articles
  • Fermina Lopez-Grondona European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD Rare Disease Working Group, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Paula Fernandez-Alvarez Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain PubMed articlesGoogle scholar articles
  • Amaia Lasa-Aranzasti Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain PubMed articlesGoogle scholar articles
  • Patricia Muñoz-Cabello Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain PubMed articlesGoogle scholar articles
  • Rika Kosaki Division of Medical Genetics, National Center for Child Health and Development, Tokyo, Japan PubMed articlesGoogle scholar articles
  • Eduardo F Tizzano Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain PubMed articlesGoogle scholar articles
  • Wendy Dewals Pediatric Cardiology Department, Antwerp University Hospital, Edegem, Belgium PubMed articlesGoogle scholar articles
  • Emma Borràs Molecular Genetics Unit, Consorci Sanitari de Terrassa, Terrassa, Spain PubMed articlesGoogle scholar articles
  • Elena Gonzalez Cañas Angiology and Vascular Surgery, Hospital Universitari Parc Tauli, Sabadell, Spain PubMed articlesGoogle scholar articles
  • Berta Almoguera European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD Rare Disease Working Group, Barcelona, Spain Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain PubMed articlesGoogle scholar articles
  • Bart Loeys Center for Medical Genetics, Antwerp University Hospital/University of Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Irene Valenzuena Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Irene Valenzuena, Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, 08035, Spain; irene.valenzuela{at}vallhebron.cat
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Citation

Totten V, Teixido-Tura G, Lopez-Grondona F, et al
Arterial aneurysm and dissection: toward the evolving phenotype of Tatton-Brown-Rahman syndrome
Journal of Medical Genetics 2024;61:870-877.

Publication history

  • Received January 8, 2024
  • Accepted June 17, 2024
  • First published July 2, 2024.
Online issue publication 
August 29, 2024

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© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.