Zobrazeno 1 - 10
of 234
pro vyhledávání: '"Left atrial isomerism"'
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 14, Iss , Pp 100472- (2023)
Background: Heterotaxy syndromes encompass left and right atrial isomerism (LAI and RAI respectively) and are associated with variable cardiac and non-cardiac anomalies which greatly influence outcomes. RAI is usually associated with complex congenit
Externí odkaz:
https://doaj.org/article/30c360c7ee50472e8d5b5dae1653c39e
Publikováno v:
Annals of Pediatric Surgery, Vol 17, Iss 1, Pp 1-4 (2021)
Abstract Background Heterotaxy syndrome is a rare clinical entity that is characterized by abnormal visceral organ arrangement in the chest and abdomen. Left atrial isomerism is a subcategory of heterotaxy syndrome characterized by the presence of mu
Externí odkaz:
https://doaj.org/article/895ad7b46e874c47952f3ec1f9e0b7f2
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Objectives: The management of atrial isomerism with complex congenital heart disease remains challenging. Experience has been largely obtained in advanced countries. The clinical diversity is greater in China. We evaluated the early- and medium-term
Externí odkaz:
https://doaj.org/article/44e2e71b683142b49e81c7246cf7a043
Publikováno v:
JACC: Case Reports, Vol 1, Iss 4, Pp 516-522 (2019)
We present the case of an infant with left atrial isomerism with complex pulmonary and systemic venous connections that resulted in physiological parallel circulation in the setting of ventriculoarterial concordance who was surgically treated using t
Externí odkaz:
https://doaj.org/article/ae5a5fbf221a4758ad48cfd109add210
Autor:
Cosmin Ioan Mohor, Sorin Radu Fleaca, Alexandra Oprinca Muja, George Calin Oprinca, Mihai Dan Roman, Radu Chicea, Adrian Gheorghe Boicean, Horatiu Dura, Ciprian Tanasescu, Nicolas Catalin Ionut Ion, Mihai Faur, Ciprian Ionut Bacila, Florina Batar, Calin Ilie Mohor
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 5, p 135 (2022)
Polysplenia syndrome represents a type of left atrial isomerism characterized by multiple small spleens, often associated with cardiac malformations and with situs ambiguus of the abdominal organs. The case presented is of a one-month-old male infant
Externí odkaz:
https://doaj.org/article/ae1c9987b9de49c8afcec6fc8f121167
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Annals of Pediatric Surgery, Vol 17, Iss 1, Pp 1-4 (2021)
BackgroundHeterotaxy syndrome is a rare clinical entity that is characterized by abnormal visceral organ arrangement in the chest and abdomen. Left atrial isomerism is a subcategory of heterotaxy syndrome characterized by the presence of multiple spl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08cae6a3ac1c9a73a8b4bc11dc7f1e41
https://doaj.org/article/895ad7b46e874c47952f3ec1f9e0b7f2
https://doaj.org/article/895ad7b46e874c47952f3ec1f9e0b7f2
Publikováno v:
Radiology Case Reports
Radiology Case Reports, Vol 16, Iss 5, Pp 1080-1084 (2021)
Radiology Case Reports, Vol 16, Iss 5, Pp 1080-1084 (2021)
Heterotaxy syndrome is a rare condition characterized by the abnormal arrangement of thoracoabdominal organs across the left-right axis of the body. It is generally classified as right and left atrial isomerism or asplenia and polysplenia syndrome, e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb8e515497fc02d26c2aa414ca527dbd
https://doi.org/10.1016/j.radcr.2021.02.015
https://doi.org/10.1016/j.radcr.2021.02.015
Publikováno v:
Acta Obstétrica e Ginecológica Portuguesa v.16 n.2 2022
Left atrial isomerism is a rare syndrome responsible for multiple cardiac, visceral and vascular malformations. Due to its high phenotype variability, prognosis can be poor. This report aims to share some unusual ultrasonographic findings of an affec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______616::ad9c4fe94fddd1e23440ced22f27953d
http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302022000200171
http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302022000200171
Publikováno v:
Cureus
Heterotaxy syndrome (HS) or situs ambiguous refers to the abnormal arrangement of viscera across the body axis, and abnormalities arise depending on the isomerism of the right or left atrial appendage. The cause remains unexplained and is attributed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87879973ffecc96a0c1cd691bdff7d0b
https://doi.org/10.7759/cureus.19055
https://doi.org/10.7759/cureus.19055