Zobrazeno 1 - 10
of 135
pro vyhledávání: '"Common atrium"'
Publikováno v:
The Cardiothoracic Surgeon, Vol 30, Iss 1, Pp 1-6 (2022)
Abstract Background Persistent left superior vena cava is a well-recognized thoracic venous abnormality, most of which do not present with any symptoms. Its opening into the left atrium is uncommonly encountered and, if present, is noted to be associ
Externí odkaz:
https://doaj.org/article/2102975bee104b3b8963b6f3842d2ad8
Identification of a novel TBX5 mutation in a Chinese family with rare symptoms of Holt–Oram syndrome
Autor:
Xia Li, Weizhe Shi, Xuejiao Ding, Jingchun Li, Yiqiang Li, Jianping Wu, Zhe Yuan, Tianying Nong, Hongwen Xu, Mingwei Zhu
Publikováno v:
Heliyon, Vol 8, Iss 11, Pp e11774- (2022)
Holt–Oram syndrome (HOS) is a rare autosomal dominant disorder characterized by skeletal abnormalities of the upper limbs and often cardiac malformations. We investigated a Chinese family with clinical features suggestive of HOS. Clinical examinati
Externí odkaz:
https://doaj.org/article/10c4ce0fe901411fab2fd752ebf4762b
Autor:
Navni Garg, Bosky Jain
Publikováno v:
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, Vol 5, Iss 1, Pp 66-69 (2021)
Common atrium (CA) is a rare congenital cardiac anomaly characterized by complete lack of interatrial septal tissue. It is commonly associated with atrioventricular valve malformations and other extracardiac anomalies. Hereby, we report a case of a t
Externí odkaz:
https://doaj.org/article/91df97a22a4c4201813dde0ab4a5f400
Publikováno v:
Clinical Case Reports, Vol 10, Iss 5, Pp n/a-n/a (2022)
Abstract Ellis–van Creveld syndrome is a rare autosomal recessive disorder caused by mutations in the EVC and EVC2 genes. The four principal manifestations are chondrodysplasia, polydactyly, ectodermal dysplasia, and congenital heart defects. We de
Externí odkaz:
https://doaj.org/article/60a411da7bd140b49e800319636d3f22
Publikováno v:
The Thoracic & Cardiovascular Surgeon Reports, Vol 09, Iss 01, Pp e4-e8 (2020)
Background A single atrium is a very rare heart condition, in which the inter atrial septum is missing. These congenital heart defects usually are surgically corrected after birth. Case Presentation We present a successful surgical repair of a single
Externí odkaz:
https://doaj.org/article/95be3fe359cd4b02b4d41bf5da8d4c30
Publikováno v:
CASE : Cardiovascular Imaging Case Reports
Graphical abstract
Highlights • Common atrium is characterized by complete/near-complete absence of IAS. • Common atrium frequently accompanies AVSD, although it can occur as an isolated entity. • Most AVSDs with an atrial communication ha
Highlights • Common atrium is characterized by complete/near-complete absence of IAS. • Common atrium frequently accompanies AVSD, although it can occur as an isolated entity. • Most AVSDs with an atrial communication ha
Autor:
Joonbum Seo, Olivier Ghez, Virginia Luis Fuentes, Tsumugi Anne Kurosawa, Poppy Bristow, Xavier Navarro-Cubas, Daniel J. Brockman
Publikováno v:
CASE : Cardiovascular Imaging Case Reports
Graphical abstract
Highlights • Large interatrial communications in dogs are rare. • When indicated, surgical closure of an interatrial communication is possible. • When indicated, surgical repair of the atrioventricular valve is possible.
Highlights • Large interatrial communications in dogs are rare. • When indicated, surgical closure of an interatrial communication is possible. • When indicated, surgical repair of the atrioventricular valve is possible.
Publikováno v:
Heart India, Vol 3, Iss 4, Pp 103-105 (2015)
Ellis-van Creveld (EVC) syndrome is a rare genetic abnormality characterized by a tetrad of chondrodysplasia, ectodermal dysplasia, polydactyly, and congenital heart disease. Common atrium is an uncommon cardiac malformation, and yet it is commonly f
Externí odkaz:
https://doaj.org/article/0468579e978e4ee681ccde22f41e46ca
Akademický článek
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Publikováno v:
Journal of Cardiac Surgery. 35:1743-1745
The association of absent right superior vena cava and persistent left superior vena cava draining into unroofed coronary sinus with common atrium and the atrioventricular septal defect is an extremely rare form of the congenital cardiac disorder wit