Zobrazeno 1 - 10
of 1 347
pro vyhledávání: '"aortopathy"'
Akademický článek
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Autor:
Hitomi Aono‐Setoguchi, Hiroki Yagi, Nana Akiyama, Norifumi Takeda, Masahiko Ando, Haruo Yamauchi, Issei Komuro, Norihiko Takeda
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message Genetic variants associated with hereditary TAAD may contribute to nonsyndromic TAAD. We present the case of a 72‐year‐old man with nonsyndromic TAAD undergoing prophylactic surgery after a gene panel test revealed a pathogen
Externí odkaz:
https://doaj.org/article/1133fb7f88084d5ab7daafe84d829de6
Autor:
Nicolas A. Stafforini, MD, Nallely Saldana-Ruiz, MD, MPH, Scott DeRoo, MD, Ulrike Schwarze, MD, Matthew P. Sweet, MD, Sara L. Zettervall, MD, MPH
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 10, Iss 4, Pp 101519- (2024)
Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome are genetic aortopathies that result from abnormal collagen matrix formation associated with vascular complications and early death. Identification of simultaneous COL3A1 and SMAD3 mutations as
Externí odkaz:
https://doaj.org/article/8041f4bd440d44c683d2aea7ad3f3f9e
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 10, p 317 (2024)
Bicuspid aortic valve disease is the most prevalent congenital heart disease, affecting up to 2% of the general population. The presentation of symptoms may vary based on the patient’s anatomy of fusion, with transthoracic echocardiography being th
Externí odkaz:
https://doaj.org/article/d51e2b2997f04dcead8ccf0ee0504031
Autor:
Osama Soliman, Yogesh Acharya, Martine Gilard, Garry Duffy, William Wijns, Venkatesh Kannan, Sherif Sultan
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
IntroductionNeural crest cells (NCCs) are multipotent and are attributed to the combination of complex multimodal gene regulatory mechanisms. Cardiac neural crest (CNC) cells, originating from the dorsal neural tube, are pivotal architects of the car
Externí odkaz:
https://doaj.org/article/ea26a7fefed143498b2ef5d799528cf1
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 15, Iss , Pp 100487- (2024)
Since the late 1980s, the standard approach for treating D-transposition of the great arteries has been the arterial switch operation (ASO), replacing the Mustard/Senning procedure. Although ASO has shown impressive long-term survival rates, recent c
Externí odkaz:
https://doaj.org/article/288eb1f3a060484f9e1ef00b830cdfad
Autor:
Jihoon Kim, MD, PhD, Jae Suk Yoo, MD, PhD, Hee-Jung Kim, MD, PhD, Ho Jin Kim, MD, Dae-Hee Kim, MD, PhD, Suk Jung Choo, MD, PhD, Joon Bum Kim, MD, PhD
Publikováno v:
JTCVS Open, Vol 15, Iss , Pp 27-37 (2023)
Objective: Genetic aortopathy, if left untreated, leads to aortic catastrophe in most affected individuals. We sought to determine the genetic mutation patterns and detection rates in patients with aortopathy and their families with a systematic scre
Externí odkaz:
https://doaj.org/article/48a4e60eb041474f9679397c6abb1e8c
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Marta Bargagna, Guido Ascione, Edoardo Zancanaro, Francesco Fioravanti, Alessandra Sala, Cinzia Trumello, Guohao Chang, Alessandro Verzini, Alessandro Castiglioni, Francesco Maisano
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 25, Iss 8, p 310 (2024)
The bicuspid aortic valve (BAV) is the most common congenital cardiac abnormality. Though most often isolated, BAV may be associated with other cardiovascular malformations. BAV-related aortopathy is the most common, sharing genetic alterations and p
Externí odkaz:
https://doaj.org/article/5b7a0e28151b4ae087634125087b2a21
Autor:
Onur B. Dolmaci, Robert J. M. Klautz, Robert E. Poelmann, Jan H. N. Lindeman, Ralf Sprengers, Lucia Kroft, Nimrat Grewal
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Introduction Bicuspid aortic valve (BAV) patients have an increased risk to develop thoracic aortic complications. Little is known about the prevalence and severity of atherosclerosis in the BAV ascending aortic wall. This study evaluates an
Externí odkaz:
https://doaj.org/article/502b9a7f321c40d9afd2c63c745a952c