Results 61 to 70 of about 17,969 (182)

Anomalous left coronary artery from the pulmonary artery presenting with aborted sudden death in an octogenarian: a case report

Journal of Medical Case Reports, 2012
Introduction We report a rare coronary anomaly presenting with aborted sudden death in an octogenarian. An anomalous left coronary artery from the pulmonary artery is a rare coronary anomaly which usually presents in the first year of life. Survival into
Separham Ahmad, Aliakbarzadeh Parvaneh
doaj   +1 more source

Splenic contraction associated with sudden, transient hypotension and sympathoexcitation in humans

Experimental Physiology, EarlyView.
Abstract The spleen is traditionally recognised for its roles in immunity and blood filtration, and it is known to contract and release stored erythrocytes in hypoxic conditions. Recent findings suggest that the spleen may also contribute to cardiovascular regulation.
Angelica Lodin‐Sundström, Gabriel Axelsson, Lisa Ljungberg, Mats H. Linér, Bodil Sjögreen, Johan P. A. Andersson   +5 more
wiley   +1 more source

Prevalence, Spectrum, and Outcomes of Single Coronary Artery Detected on Coronary Computed Tomography Angiography (CCTA)

Radiology Research and Practice, 2019
Background. Single coronary artery (SCA) is a rare congenital anomaly in which there is an isolated coronary artery that arises from a single coronary ostium and provides coronary blood supply to the entire myocardium.
Rashid Al Umairi, Maryam Al-khouri
doaj   +1 more source

Congenital anomalies of the coronary arteries.

Revista portuguesa de cardiologia, 2018
Congenital coronary artery anomalies are modifications of their origin, course or structure and its incidence varies between 0,2 and 5,6% of the general population. Although the majority is asymptomatic, they are the second leading cause of sudden cardiac death in young athletes. The aim of this study is to highlight the main anomalies with hemodynamic
Silva, Andreia, Baptista, Maria João, Araújo, Emanuel   +2 more
openaire   +2 more sources

Standardized Reporting of Cardiac Magnetic Resonance Examinations in Children With Cardiac Diseases and Adults With Congenital Heart Disease: A Scientific Statement From the Association for European Pediatric and Congenital Cardiology (AEPC) and the International Society for Magnetic Resonance in Medicine (ISMRM)

Journal of Magnetic Resonance Imaging, EarlyView.
Francesca Raimondi, Inga Voges, Lamia Ait‐Ali, Sonya Babu‐Narayan, Rene Botnar, Barbara Burkhardt, Adrienne Campbell‐Washburn, Dominik Daniel Gabbert, Georg Hansmann, Willem A. Helbing, Hasan Hosan, Sylvia Krupickova, Heiner Latus, Duarte Martins, Colin McMahon, Christian Meierhofer, Vivek Muthurangu, Tiina Ojala, Pim van Ooij, Claudia Prieto, Milan Prsa, Kuberan Pushparajah, José F. Rodríguez Palomares, Samir Sarikouch, Lars Grosse‐Wortman, F. Gerald Greil, Heynric Grotenhuis   +26 more
wiley   +1 more source

Congenital heart disease in pregnancy and severe maternal morbidity: A distributed data network study

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract Introduction Pregnant people with congenital heart disease (CHD) are a growing patient population in obstetrics, yet evidence on the risk for severe maternal morbidity (SMM) has largely been limited to studies that lack specificity for CHD. We conducted this study to demonstrate the utility of distributed data networks for obstetric research ...
Elizabeth B. Sherwin, Benjamin Martin, Xiao Xu, Anna Booman, Alyssa Howren, Kimberlee McKay, Sadaf Kazi, Sean O'Reilly, Katie S. Kolla, Khyzer Aziz, Katherine Bianco, Stephanie A. Leonard   +11 more
wiley   +1 more source

Successful Surgical Treatment of a Septuagenarian with Anomalous Right Coronary Artery from the Pulmonary Artery with an Eleven Year Follow-Up : Case report and review of literature

Sultan Qaboos University Medical Journal, 2013
An anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a very rare coronary artery anomaly with only 98 cases reported in literature till date.
Paresh Kumar Kuba, Jasvinder Sharma, Ashok Sharma   +2 more
doaj  

A New Variant of Dual Left Anterior Descending Artery Anomaly: Type XI

Sultan Qaboos University Medical Journal, 2018
A dual left anterior descending (LAD) artery is a rare congenital anomaly which is classified into different types based on the origin, course and termination of the short and long LAD arteries. To date, 10 variants of dual LAD artery anomalies have been
Rashid S. Al-Umairi, Faiza A. Al-Kindi, Saqar A. Al-Tai   +2 more
doaj   +1 more source

Congenital Coronary Artery Anomalies

Journal of the Korean Society of Radiology
See the article, “Type 4 Dual Left Anterior Descending Artery: A Case Report of a Rare Congenital Coronary Anomaly”, in volume 85 on page 428-433 (https://doi. org/10.3348/ jksr.2022.0147).
openaire   +3 more sources

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1783-1798, August 2026.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source