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Expert Review of Cardiovascular Therapy Volume 17, 2019 - Issue 12
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Review

Features of Marfan syndrome not listed in the Ghent nosology – the dark side of the disease

Yskert von Kodolitscha German Aorta Center Hamburg at University Hospital Hamburg Eppendorf University Heart Centre, Clinics for Cardiology and Heart Surgery, VASCERN HTAD European Reference CentreCorrespondence[email protected]
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Anthony Demolderb Center for Medical Genetics and Department of Cardiology, Ghent University Hospital, VASCERN HTAD European Reference Centre, Ghent, BelgiumView further author information
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Evaldas Girdauskasa German Aorta Center Hamburg at University Hospital Hamburg Eppendorf University Heart Centre, Clinics for Cardiology and Heart Surgery, VASCERN HTAD European Reference CentreView further author information
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Harald Kaemmererc Department of Pediatric Cardiology and Congenital Heart Disease, German Heart Centre Munich of the Free State of Bavaria, MunichView further author information
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Katharina Kornhuberc Department of Pediatric Cardiology and Congenital Heart Disease, German Heart Centre Munich of the Free State of Bavaria, MunichView further author information
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Laura Muino Mosquerad Department of Pediatric Cardiology and Center for Medical Genetics, Ghent University Hospital, Ghent, BelgiumView further author information
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Shaine Morrise Department of Pediatrics-Cardiology, Texas Children’s Hospital/Baylor College of Medicine, Houston, TX, USAView further author information
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Enid Neptunef Division of Pulmonary and Critical Care Medicine and Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USAView further author information
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Reed Pyeritzg Departments of Medicine and Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USAView further author information
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Svend Rand-Hendriksenh TRS, National Resource Centre for Rare Disorders, Sunnaas Rehabilitation Hospital, Nesoddtangen, NorwayView further author information
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Alexander Rahmani Department of Conservative Dentistry, Periodontology and Preventive Dentistry, Hannover Medical School, HannoverView further author information
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Nina Riiseh TRS, National Resource Centre for Rare Disorders, Sunnaas Rehabilitation Hospital, Nesoddtangen, NorwayView further author information
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Leema Robertj Department of Clinical Genetics, Guy’s and St Thomas’ NHS Foundation Trust, London, UKView further author information
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Ingmar Staufenbieli Department of Conservative Dentistry, Periodontology and Preventive Dentistry, Hannover Medical School, HannoverView further author information
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Katalin Szöcsa German Aorta Center Hamburg at University Hospital Hamburg Eppendorf University Heart Centre, Clinics for Cardiology and Heart Surgery, VASCERN HTAD European Reference CentreView further author information
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Thy Thy Vanemh TRS, National Resource Centre for Rare Disorders, Sunnaas Rehabilitation Hospital, Nesoddtangen, Norway;k Department of Physical Medicine and Rehabilitation, Oslo University Hospital, Oslo, NorwayView further author information
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Stephan J. Linkel Clinic of Ophthalmology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany;m Ophthalmological practice at the University Clinic Hamburg-Eppendorf, zentrumsehstärke, Hamburg, GermanyView further author information
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Marina Voglern German Marfan Association, Marfan Hilfe Deutschland e.V, Eutin, GermanyView further author information
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Anji Yetmano Vascular Medicine, Children’s Hospital and Medical Center, Omaha, USAView further author information
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Julie De Backerb Center for Medical Genetics and Department of Cardiology, Ghent University Hospital, VASCERN HTAD European Reference Centre, Ghent, BelgiumView further author information
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Pages 883-915 | Received 09 Sep 2019, Accepted 11 Dec 2019, Published online: 08 Jan 2020

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