Published Erratum
doi: 10.1038/s41436-018-0035-3.
Correction: Arterial tortuosity syndrome: 40 new families and literature review
Aude Beyens
1
, Juliette Albuisson
2
, Annekatrien Boel
1
, Mazen Al-Essa
3
, Waheed Al-Manea
4
, Damien Bonnet
5
, Ozlem Bostan
6
, Odile Boute
7
, Tiffany Busa
8
, Nathalie Canham
9
, Ergun Cil
6
, Paul J Coucke
1
, Margot A Cousin
10
11
, Majed Dasouki
12
, Julie De Backer
1
13
, Anne De Paepe
1
, Sofie De Schepper
14
, Deepthi De Silva
15
16
, Koenraad Devriendt
17
, Inge De Wandele
1
, David R Deyle
10
18
19
, Harry Dietz
20
, Sophie Dupuis-Girod
21
, Eudice Fontenot
22
, Björn Fischer-Zirnsak
23
, Alper Gezdirici
24
, Jamal Ghoumid
25
, Fabienne Giuliano
26
, Neus Baena
27
, Mohammed Z Haider
3
, Joshua S Hardin
28
, Xavier Jeunemaitre
2
, Eric W Klee
8
9
18
, Uwe Kornak
23
, Manuel F Landecho
29
, Anne Legrand
2
, Bart Loeys
30
, Stanislas Lyonnet
5
, Helen Michael
31
, Pamela Moceri
32
, Shehla Mohammed
33
, Laura Muiño-Mosquera
1
, Sheela Nampoothiri
34
, Karin Pichler
35
, Katrina Prescott
36
, Anna Rajeb
23
, Maria Ramos-Arroyo
37
, Massimiliano Rossi
38
, Mustafa Salih
39
, Mohammed Z Seidahmed
4
, Elise Schaefer
40
, Elisabeth Steichen-Gersdorf
35
, Sehime Temel
41
42
43
, Fahrettin Uysal
6
, Marine Vanhomwegen
1
, Lut Van Laer
30
, Lionel Van Maldergem
44
, David Warner
28
, Andy Willaert
1
, Tom R Collins Ii
22
, Andrea Taylor
45
, Elaine C Davis
46
, Yuri Zarate
10
, Bert Callewaert
47
Affiliations
Affiliations
- 1 Center For Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
- 2 APH, Hôpital Européen Georges Pompidou, Centre de Référence des Maladies Vasculaires Rares, INSERM, U970, Université Descartes Paris, Sarbonne Cité, Paris, France.
- 3 Pediatrics Department, Kuwait University, Kuwait City, Kuwait.
- 4 Pediatric Department, Security Forces Hospital, Riyadh, Saudi Arabia.
- 5 Medical Genetics Service, Hôpital Necker-Enfants Malades, Paris, France.
- 6 Department of Pediatric Cardiology, University of Uludag, Bursa, Turkey.
- 7 Clinical Genetics Service "Guy Fontaine," Hôpital Calmette, Lille, France.
- 8 Service de Génétique Clinique, Département de Génétique, AP-HM CHU Timone Enfants, Marseille, France.
- 9 North West Thames Regional Genetics Service, Northwick Park Hospital, Harrow, United Kingdom.
- 10 Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
- 11 Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
- 12 Department of Pediatrics, University of Kansas, Kansas City, Kansas, USA.
- 13 Department of Cardiology, Ghent University Hospital, Ghent, Belgium.
- 14 Department of Dermatology, Ghent University Hospital, Ghent, Belgium.
- 15 Department of Physiology, University of Kelaniya, Ragama, Sri Lanka.
- 16 Faculty of Medicine, University of Kelaniya, Ragama, Sri Lanka.
- 17 Center for Human Genetics, Leuven University Hospital, Leuven, Belgium.
- 18 Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.
- 19 Department of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
- 20 Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
- 21 Hospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Service de Génétique et Centre de Référence Pour la Maladie de Rendu-Osler, Université Lyon, Lyon, France.
- 22 Division of Cardiology, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
- 23 Institute of Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany.
- 24 Department of Medical Genetics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
- 25 Department of Medical Genetics, Lille University Hospital, CHU Lille, Lille, France.
- 26 Department of Physical Medicine and Rehabilitation, Raymond Poincare Hospital, Garches, France.
- 27 Genetics Laboratory UDIAT Diagnostic Center, Parc Tauli University Hospital, Sabadell, Spain.
- 28 Department of Ophthalmology, Arkansas Children's Hospital, Little Rock, Arkansas, USA.
- 29 Department of Internal Medicine, Clínica Universidad de Navarra, Pamplona, Spain.
- 30 Center of Medical Genetics, University Hospital of Antwerp, Antwerp, Belgium.
- 31 Paediatric Cardiology and Transition, Leeds General Infirmary, Leeds, United Kingdom.
- 32 Cardiology Department, Université Côte d'Azur, CHU de Nice et Hôpitaux Universitaires Pédiatriques Lenval, Nice, France.
- 33 South East Thames Regional Genetics Service, Guy's Hospital, London, United Kingdom.
- 34 Department of Pediatric Genetics, Amrita Institute of Medical Sciences and Research Center, Cochin, Kerala, India.
- 35 Clinic for Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.
- 36 Clinical Genetics, Yorkshire Regional Genetics Service, Leeds, United Kingdom.
- 37 Medical Genetics Service, Complejo Hospitalario de Navarra, Pamplona, Spain.
- 38 Genetic Department, Femme-Mère-Enfant Hospital, Hospices Civils de Lyon and INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Université Claude Bernard Lyon 1, Bron, France.
- 39 Division of Pediatric Neurology, King Saud University, Riyadh, Saudi Arabia.
- 40 Medical Genetics Service, CHU Strasbourg, Strasbourg, France.
- 41 Department of Histology and Embryology, Faculty of Medicine, Near East University, Lefkoşa, Cyprus.
- 42 Department of Histology and Embryology, Faculty of Medicine, University of Uludag, Bursa, Turkey.
- 43 Department of Medical Genetics, Faculty of Medicine, University of Uludag, Bursa, Turkey.
- 44 Centre for Human Genetics, Université de Franche Comté, Besançon, France.
- 45 A Twist of Fate-ATS, Owasso, Oklahoma, USA.
- 46 Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.
- 47 Center For Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium. bert.callewaert@ugent.be.
- PMID: 30201961
- DOI: 10.1038/s41436-018-0035-3
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Published Erratum
Correction: Arterial tortuosity syndrome: 40 new families and literature review
Aude Beyens et al.
Genet Med.
2019 Aug.
Free article
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doi: 10.1038/s41436-018-0035-3.
Authors
Aude Beyens
1
, Juliette Albuisson
2
, Annekatrien Boel
1
, Mazen Al-Essa
3
, Waheed Al-Manea
4
, Damien Bonnet
5
, Ozlem Bostan
6
, Odile Boute
7
, Tiffany Busa
8
, Nathalie Canham
9
, Ergun Cil
6
, Paul J Coucke
1
, Margot A Cousin
10
11
, Majed Dasouki
12
, Julie De Backer
1
13
, Anne De Paepe
1
, Sofie De Schepper
14
, Deepthi De Silva
15
16
, Koenraad Devriendt
17
, Inge De Wandele
1
, David R Deyle
10
18
19
, Harry Dietz
20
, Sophie Dupuis-Girod
21
, Eudice Fontenot
22
, Björn Fischer-Zirnsak
23
, Alper Gezdirici
24
, Jamal Ghoumid
25
, Fabienne Giuliano
26
, Neus Baena
27
, Mohammed Z Haider
3
, Joshua S Hardin
28
, Xavier Jeunemaitre
2
, Eric W Klee
8
9
18
, Uwe Kornak
23
, Manuel F Landecho
29
, Anne Legrand
2
, Bart Loeys
30
, Stanislas Lyonnet
5
, Helen Michael
31
, Pamela Moceri
32
, Shehla Mohammed
33
, Laura Muiño-Mosquera
1
, Sheela Nampoothiri
34
, Karin Pichler
35
, Katrina Prescott
36
, Anna Rajeb
23
, Maria Ramos-Arroyo
37
, Massimiliano Rossi
38
, Mustafa Salih
39
, Mohammed Z Seidahmed
4
, Elise Schaefer
40
, Elisabeth Steichen-Gersdorf
35
, Sehime Temel
41
42
43
, Fahrettin Uysal
6
, Marine Vanhomwegen
1
, Lut Van Laer
30
, Lionel Van Maldergem
44
, David Warner
28
, Andy Willaert
1
, Tom R Collins Ii
22
, Andrea Taylor
45
, Elaine C Davis
46
, Yuri Zarate
10
, Bert Callewaert
47
Affiliations
- 1 Center For Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
- 2 APH, Hôpital Européen Georges Pompidou, Centre de Référence des Maladies Vasculaires Rares, INSERM, U970, Université Descartes Paris, Sarbonne Cité, Paris, France.
- 3 Pediatrics Department, Kuwait University, Kuwait City, Kuwait.
- 4 Pediatric Department, Security Forces Hospital, Riyadh, Saudi Arabia.
- 5 Medical Genetics Service, Hôpital Necker-Enfants Malades, Paris, France.
- 6 Department of Pediatric Cardiology, University of Uludag, Bursa, Turkey.
- 7 Clinical Genetics Service "Guy Fontaine," Hôpital Calmette, Lille, France.
- 8 Service de Génétique Clinique, Département de Génétique, AP-HM CHU Timone Enfants, Marseille, France.
- 9 North West Thames Regional Genetics Service, Northwick Park Hospital, Harrow, United Kingdom.
- 10 Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
- 11 Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
- 12 Department of Pediatrics, University of Kansas, Kansas City, Kansas, USA.
- 13 Department of Cardiology, Ghent University Hospital, Ghent, Belgium.
- 14 Department of Dermatology, Ghent University Hospital, Ghent, Belgium.
- 15 Department of Physiology, University of Kelaniya, Ragama, Sri Lanka.
- 16 Faculty of Medicine, University of Kelaniya, Ragama, Sri Lanka.
- 17 Center for Human Genetics, Leuven University Hospital, Leuven, Belgium.
- 18 Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.
- 19 Department of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
- 20 Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
- 21 Hospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Service de Génétique et Centre de Référence Pour la Maladie de Rendu-Osler, Université Lyon, Lyon, France.
- 22 Division of Cardiology, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
- 23 Institute of Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany.
- 24 Department of Medical Genetics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
- 25 Department of Medical Genetics, Lille University Hospital, CHU Lille, Lille, France.
- 26 Department of Physical Medicine and Rehabilitation, Raymond Poincare Hospital, Garches, France.
- 27 Genetics Laboratory UDIAT Diagnostic Center, Parc Tauli University Hospital, Sabadell, Spain.
- 28 Department of Ophthalmology, Arkansas Children's Hospital, Little Rock, Arkansas, USA.
- 29 Department of Internal Medicine, Clínica Universidad de Navarra, Pamplona, Spain.
- 30 Center of Medical Genetics, University Hospital of Antwerp, Antwerp, Belgium.
- 31 Paediatric Cardiology and Transition, Leeds General Infirmary, Leeds, United Kingdom.
- 32 Cardiology Department, Université Côte d'Azur, CHU de Nice et Hôpitaux Universitaires Pédiatriques Lenval, Nice, France.
- 33 South East Thames Regional Genetics Service, Guy's Hospital, London, United Kingdom.
- 34 Department of Pediatric Genetics, Amrita Institute of Medical Sciences and Research Center, Cochin, Kerala, India.
- 35 Clinic for Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.
- 36 Clinical Genetics, Yorkshire Regional Genetics Service, Leeds, United Kingdom.
- 37 Medical Genetics Service, Complejo Hospitalario de Navarra, Pamplona, Spain.
- 38 Genetic Department, Femme-Mère-Enfant Hospital, Hospices Civils de Lyon and INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Université Claude Bernard Lyon 1, Bron, France.
- 39 Division of Pediatric Neurology, King Saud University, Riyadh, Saudi Arabia.
- 40 Medical Genetics Service, CHU Strasbourg, Strasbourg, France.
- 41 Department of Histology and Embryology, Faculty of Medicine, Near East University, Lefkoşa, Cyprus.
- 42 Department of Histology and Embryology, Faculty of Medicine, University of Uludag, Bursa, Turkey.
- 43 Department of Medical Genetics, Faculty of Medicine, University of Uludag, Bursa, Turkey.
- 44 Centre for Human Genetics, Université de Franche Comté, Besançon, France.
- 45 A Twist of Fate-ATS, Owasso, Oklahoma, USA.
- 46 Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.
- 47 Center For Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium. bert.callewaert@ugent.be.
- PMID: 30201961
- DOI: 10.1038/s41436-018-0035-3
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Abstract
In the published version of this paper the author Neus Baena's name was incorrectly given as Neus Baena Diez. This has now been corrected in both the HTML and PDF versions of the paper.
Erratum for
-
Arterial tortuosity syndrome: 40 new families and literature review.Beyens A, Albuisson J, Boel A, Al-Essa M, Al-Manea W, Bonnet D, Bostan O, Boute O, Busa T, Canham N, Cil E, Coucke PJ, Cousin MA, Dasouki M, De Backer J, De Paepe A, De Schepper S, De Silva D, Devriendt K, De Wandele I, Deyle DR, Dietz H, Dupuis-Girod S, Fontenot E, Fischer-Zirnsak B, Gezdirici A, Ghoumid J, Giuliano F, Diéz NB, Haider MZ, Hardin JS, Jeunemaitre X, Klee EW, Kornak U, Landecho MF, Legrand A, Loeys B, Lyonnet S, Michael H, Moceri P, Mohammed S, Muiño-Mosquera L, Nampoothiri S, Pichler K, Prescott K, Rajeb A, Ramos-Arroyo M, Rossi M, Salih M, Seidahmed MZ, Schaefer E, Steichen-Gersdorf E, Temel S, Uysal F, Vanhomwegen M, Van Laer L, Van Maldergem L, Warner D, Willaert A, Collins TR, Taylor A, Davis EC, Zarate Y, Callewaert B. Beyens A, et al. Genet Med. 2018 Oct;20(10):1236-1245. doi: 10.1038/gim.2017.253. Epub 2018 Jan 11. Genet Med. 2018. PMID: 29323665
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