Mitral valve prolapse and aortic root dilation in adults with hypermobile Ehlers–Danlos syndrome and related disorders

2018 ◽  
Vol 176 (9) ◽  
pp. 1838-1844 ◽  
Author(s):  
Stephanie B. Asher ◽  
Rensa Chen ◽  
Staci Kallish
2022 ◽  
pp. 1358863X2110675
Author(s):  
Eman R Rashed ◽  
Tania Ruiz Maya ◽  
Jennifer Black ◽  
Veronica Fettig ◽  
Daniella Kadian-Dodov ◽  
...  

Introduction: Mitral valve prolapse and aortic root dilatation are reported in association with hypermobile Ehlers–Danlos syndrome (hEDS), but the full phenotypic spectrum of cardiovascular complications in this condition has not been studied in the aftermath of updated nosology and diagnostic criteria. Methods: We performed a retrospective review of 258 patients (> 94% adults) referred to a multidisciplinary clinic for evaluation of joint hypermobility between January 2017 and December 2020 and diagnosed with hEDS or a hypermobility spectrum disorder (HSD) to determine the incidence and spectrum of cardiovascular involvement. Results: Mitral valve prolapse was present in 7.5% and thoracic aortic dilatation in 15.2%. Aortic dilatation was more frequent in individuals with hEDS (20.7%) than with HSD (7.7%) and similarly prevalent between males and females, although was mild in > 90% of females and moderate-to-severe in 50% of males. Five individuals (1.9%) with hEDS/HSD had extra-aortic arterial involvement, including cervical artery dissection (CeAD, n = 2), spontaneous coronary artery dissection (SCAD, n = 2), and SCAD plus celiac artery pseudoaneurysm ( n = 1). This is the first series to report the prevalence of CeAD and SCAD in hEDS/HSD. Conclusions: Cardiovascular manifestations in adults with hEDS/HSD, especially females, are typically mild and readily assessed by echocardiography. Since the risk of progression has not yet been defined, adults with hEDS/HSD who are found to have aortic dilatation at baseline should continue ongoing surveillance to monitor for progressive dilatation. Cardiovascular medicine specialists, neurologists, and neurosurgeons should consider hEDS/HSD on the differential for patients with CeAD or SCAD who also have joint hypermobility.


2002 ◽  
Vol 31 (4) ◽  
pp. 288-291
Author(s):  
Hiroshi Kumano ◽  
Akimitsu Yamaguchi ◽  
Tatsuya Kiji ◽  
Hiroyuki Maruhashi ◽  
Satoshi Kato

2008 ◽  
Vol 53 (6) ◽  
pp. 460-465 ◽  
Author(s):  
George E. Tiller ◽  
Suzanne B. Cassidy ◽  
Christine Wensel ◽  
Richard J. Wenstrup

2014 ◽  
Vol 25 (2) ◽  
pp. 365-367 ◽  
Author(s):  
Takaya Hoashi ◽  
Isao Shiraishi ◽  
Hajime Ichikawa

AbstractA 21-year-old man underwent mitral valve replacement and tricuspid annuloplasty for severe mitral regurgitation and moderate tricuspid regurgitation. Until the operation, he had been treated for hypermobility type Ehlers–Danlos syndrome. Gene examination revealed a mutation in filamin A gene, which is the gene responsible for X-linked myxomatous valvular dystrophy.


2018 ◽  
Vol 10 (1) ◽  
pp. 107
Author(s):  
S. Zarka ◽  
A. Rossi ◽  
S. Abouth ◽  
M. Frank ◽  
G. Goudot ◽  
...  

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