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

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Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease. / von Kodolitsch, Yskert; Demolder, Anthony; Girdauskas, Evaldas; Kaemmerer, Harald; Kornhuber, Katharina; Muino Mosquera, Laura; Morris, Shaine; Neptune, Enid; Pyeritz, Reed; Rand-Hendriksen, Svend; Rahman, Alexander; Riise, Nina; Robert, Leema; Staufenbiel, Ingmar; Szöcs, Katalin; Vanem, Thy Thy; Linke, Stephan J; Vogler, Marina; Yetman, Anji; De Backer, Julie.

In: EXPERT REV CARDIOVAS, Vol. 17, No. 12, 12.2019, p. 883-915.

Research output: SCORING: Contribution to journal › SCORING: Review article › Research

Harvard

von Kodolitsch, Y, Demolder, A, Girdauskas, E, Kaemmerer, H, Kornhuber, K, Muino Mosquera, L, Morris, S, Neptune, E, Pyeritz, R, Rand-Hendriksen, S, Rahman, A, Riise, N, Robert, L, Staufenbiel, I, Szöcs, K, Vanem, TT, Linke, SJ, Vogler, M, Yetman, A & De Backer, J 2019, 'Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease', EXPERT REV CARDIOVAS, vol. 17, no. 12, pp. 883-915. https://doi.org/10.1080/14779072.2019.1704625

APA

von Kodolitsch, Y., Demolder, A., Girdauskas, E., Kaemmerer, H., Kornhuber, K., Muino Mosquera, L., Morris, S., Neptune, E., Pyeritz, R., Rand-Hendriksen, S., Rahman, A., Riise, N., Robert, L., Staufenbiel, I., Szöcs, K., Vanem, T. T., Linke, S. J., Vogler, M., Yetman, A., & De Backer, J. (2019). Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease. EXPERT REV CARDIOVAS, 17(12), 883-915. https://doi.org/10.1080/14779072.2019.1704625

Vancouver

von Kodolitsch Y, Demolder A, Girdauskas E, Kaemmerer H, Kornhuber K, Muino Mosquera L et al. Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease. EXPERT REV CARDIOVAS. 2019 Dec;17(12):883-915. https://doi.org/10.1080/14779072.2019.1704625

Bibtex

@article{6642318caf21439eb3c00799c351c64d,
title = "Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease",
abstract = "Introduction: The revised Ghent nosology presents the classical features of Marfan syndrome. However, behind its familiar face, Marfan syndrome hides less well-known features.Areas covered: The German Marfan Organization listed unusual symptoms and clinical experts reviewed the literature on clinical features of Marfan syndrome not listed in the Ghent nosology. Thereby we identified the following features: (1) bicuspid aortic valve, mitral valve prolapse, pulmonary valve prolapse, tricuspid valve prolapse, (2) heart failure and cardiomyopathy, (3) supraventricular arrhythmia, ventricular arrhythmia, and abnormal repolarization, (4) spontaneous coronary artery dissection, anomalous coronary arteries, and atherosclerotic coronary artery disease, tortuosity-, aneurysm-, and dissection of large and medium-sized arteries, (5) restrictive lung disease, parenchymal lung disease, and airway disorders, (6) obstructive- and central sleep apnea, (7) liver and kidney cysts, biliary tract disease, diaphragmatic hernia, and adiposity, (8) premature labor, and urinary incontinence, (9) myopathy, reduced bone mineral density, and craniofacial manifestations, (10) atrophic scars, (11) caries, and craniomandibular dysfunction, (12) headache from migraine and spontaneous cerebrospinal fluid leakage, (13) cognitive dysfunction, schizophrenia, depression, fatigue, and pain, (14) and activated fibrinolysis, thrombin, platelets, acquired von Willebrand disease, and platelet dysfunction.Expert commentary: Future research, nosologies, and guidelines may consider less well-known features of Marfan syndrome.",
keywords = "Bone and Bones/pathology, Cardiovascular Diseases/etiology, Humans, Lung/physiopathology, Marfan Syndrome/physiopathology",
author = "{von Kodolitsch}, Yskert and Anthony Demolder and Evaldas Girdauskas and Harald Kaemmerer and Katharina Kornhuber and {Muino Mosquera}, Laura and Shaine Morris and Enid Neptune and Reed Pyeritz and Svend Rand-Hendriksen and Alexander Rahman and Nina Riise and Leema Robert and Ingmar Staufenbiel and Katalin Sz{\"o}cs and Vanem, {Thy Thy} and Linke, {Stephan J} and Marina Vogler and Anji Yetman and {De Backer}, Julie",
year = "2019",
month = dec,
doi = "10.1080/14779072.2019.1704625",
language = "English",
volume = "17",
pages = "883--915",
journal = "EXPERT REV CARDIOVAS",
issn = "1477-9072",
publisher = "Taylor and Francis Ltd.",
number = "12",

}

RIS

TY - JOUR

T1 - Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease

AU - von Kodolitsch, Yskert

AU - Demolder, Anthony

AU - Girdauskas, Evaldas

AU - Kaemmerer, Harald

AU - Kornhuber, Katharina

AU - Muino Mosquera, Laura

AU - Morris, Shaine

AU - Neptune, Enid

AU - Pyeritz, Reed

AU - Rand-Hendriksen, Svend

AU - Rahman, Alexander

AU - Riise, Nina

AU - Robert, Leema

AU - Staufenbiel, Ingmar

AU - Szöcs, Katalin

AU - Vanem, Thy Thy

AU - Linke, Stephan J

AU - Vogler, Marina

AU - Yetman, Anji

AU - De Backer, Julie

PY - 2019/12

Y1 - 2019/12

N2 - Introduction: The revised Ghent nosology presents the classical features of Marfan syndrome. However, behind its familiar face, Marfan syndrome hides less well-known features.Areas covered: The German Marfan Organization listed unusual symptoms and clinical experts reviewed the literature on clinical features of Marfan syndrome not listed in the Ghent nosology. Thereby we identified the following features: (1) bicuspid aortic valve, mitral valve prolapse, pulmonary valve prolapse, tricuspid valve prolapse, (2) heart failure and cardiomyopathy, (3) supraventricular arrhythmia, ventricular arrhythmia, and abnormal repolarization, (4) spontaneous coronary artery dissection, anomalous coronary arteries, and atherosclerotic coronary artery disease, tortuosity-, aneurysm-, and dissection of large and medium-sized arteries, (5) restrictive lung disease, parenchymal lung disease, and airway disorders, (6) obstructive- and central sleep apnea, (7) liver and kidney cysts, biliary tract disease, diaphragmatic hernia, and adiposity, (8) premature labor, and urinary incontinence, (9) myopathy, reduced bone mineral density, and craniofacial manifestations, (10) atrophic scars, (11) caries, and craniomandibular dysfunction, (12) headache from migraine and spontaneous cerebrospinal fluid leakage, (13) cognitive dysfunction, schizophrenia, depression, fatigue, and pain, (14) and activated fibrinolysis, thrombin, platelets, acquired von Willebrand disease, and platelet dysfunction.Expert commentary: Future research, nosologies, and guidelines may consider less well-known features of Marfan syndrome.

AB - Introduction: The revised Ghent nosology presents the classical features of Marfan syndrome. However, behind its familiar face, Marfan syndrome hides less well-known features.Areas covered: The German Marfan Organization listed unusual symptoms and clinical experts reviewed the literature on clinical features of Marfan syndrome not listed in the Ghent nosology. Thereby we identified the following features: (1) bicuspid aortic valve, mitral valve prolapse, pulmonary valve prolapse, tricuspid valve prolapse, (2) heart failure and cardiomyopathy, (3) supraventricular arrhythmia, ventricular arrhythmia, and abnormal repolarization, (4) spontaneous coronary artery dissection, anomalous coronary arteries, and atherosclerotic coronary artery disease, tortuosity-, aneurysm-, and dissection of large and medium-sized arteries, (5) restrictive lung disease, parenchymal lung disease, and airway disorders, (6) obstructive- and central sleep apnea, (7) liver and kidney cysts, biliary tract disease, diaphragmatic hernia, and adiposity, (8) premature labor, and urinary incontinence, (9) myopathy, reduced bone mineral density, and craniofacial manifestations, (10) atrophic scars, (11) caries, and craniomandibular dysfunction, (12) headache from migraine and spontaneous cerebrospinal fluid leakage, (13) cognitive dysfunction, schizophrenia, depression, fatigue, and pain, (14) and activated fibrinolysis, thrombin, platelets, acquired von Willebrand disease, and platelet dysfunction.Expert commentary: Future research, nosologies, and guidelines may consider less well-known features of Marfan syndrome.

KW - Bone and Bones/pathology

KW - Cardiovascular Diseases/etiology

KW - Humans

KW - Lung/physiopathology

KW - Marfan Syndrome/physiopathology

U2 - 10.1080/14779072.2019.1704625

DO - 10.1080/14779072.2019.1704625

M3 - SCORING: Review article

C2 - 31829751

VL - 17

SP - 883

EP - 915

JO - EXPERT REV CARDIOVAS

JF - EXPERT REV CARDIOVAS

SN - 1477-9072

IS - 12

ER -