Cardiovascular Management of Aortopathy in Children: A Scientific Statement From the American Heart Association
SA Morris, JN Flyer, AT Yetman, E Quezada… - Circulation, 2024 - ahajournals.org
Aortopathy encompasses a spectrum of conditions predisposing to dilation, aneurysm,
dissection, or rupture of the aorta and other blood vessels. Aortopathy is diagnosed …
dissection, or rupture of the aorta and other blood vessels. Aortopathy is diagnosed …
In vivo phenotypic vascular dysfunction extends beyond the aorta in a mouse model for fibrillin-1 (Fbn1) mutation
T Curry, ME Barrameda, TC Thomas, M Esfandiarei - Scientific Reports, 2024 - nature.com
Abstract In individuals with Marfan Syndrome (MFS), fibrillin-1 gene (FBN1) mutations can
lead to vascular wall weakening and dysfunction. The experimental mouse model of MFS …
lead to vascular wall weakening and dysfunction. The experimental mouse model of MFS …
Vascular Ehlers-Danlos syndrome with a Novel missense COL3A1 gene mutation present with bilateral spontaneous carotid-cavernous fistula: a case report
K Tatebayashi, M Shirakawa, S Abe, M Fujita… - Acta …, 2023 - Springer
This report describes a unique case of vascular Ehlers-Danlos syndrome (vEDS)
characterized by multiple spontaneous direct carotid-cavernous sinus fistulas (CCF). The …
characterized by multiple spontaneous direct carotid-cavernous sinus fistulas (CCF). The …
Endovascular intervention to treat spontaneous carotid-cavernous fistula in a patient with Ehlers-Danlos Syndrome with an access site anatomical variant
AJX See, AH Ashok, Y Joshi, M Guilfoyle… - BJR| Case …, 2024 - academic.oup.com
Abstract Vascular Ehlers-Danlos Syndrome (vEDS) is a rare and potentially life-threatening
inherited connective tissue disorder. Patients with vEDS can present with spontaneous …
inherited connective tissue disorder. Patients with vEDS can present with spontaneous …
[PDF][PDF] PMC10924961.
T Curry, ME Barrameda, TC Thomas… - … BRAIN INJURY IN …, 2024 - repository.arizona.edu
In individuals with Marfan Syndrome (MFS), fibrillin-1 gene (Fbn1) mutations can lead to
vascular wall weakening and dysfunction. The experimental mouse model of MFS …
vascular wall weakening and dysfunction. The experimental mouse model of MFS …
血管型Ehlers-Danlos 症候群に合併した内頚動脈海綿静脈洞瘻に対してTVE を施行した1 例
中江竜太， 金子純也， 金谷貴大， 久保田麻紗美… - 脳卒中の外科, 2024 - jstage.jst.go.jp
抄録 血管型 Ehlers-Danlos 症候群 (vEDS) は内頚動脈海綿静脈洞瘻 (CCF) を合併する.
今回われわれは vEDS に合併した CCF に対して TVE を施行した症例を経験したので報告する …
今回われわれは vEDS に合併した CCF に対して TVE を施行した症例を経験したので報告する …