Results 121 to 130 of about 38,605 (290)
Journal of Genetic Counseling, Volume 34, Issue 3, June 2025.Abstract Hypertrophic cardiomyopathy (HCM) is a common hereditary condition affecting approximately 1 in 500 adults. It is characterized by marked clinical heterogeneity with individuals experiencing minimal to no symptoms, while others may have more severe outcomes including heart failure and sudden cardiac death.
Erin M. Miller +7 more
wiley +1 more source
, 2010 VACTERL association is a useful acronym for a condition characterised by the sporadic, non-random association of specific birth defects of multiple organ systems.We present one such case which had congenital abnormalities of renal,skeletal and cardiac ...
Rabah, SM, Salati, SA
core +1 more source
A Rare Case of Huge Cardiomegaly
Journal of the American College of Cardiology, 2012 ![Figure][1] [![Graphic][3] ][3][![Graphic][4] ][4] A 40-year-old male with history of rheumatic heart disease presented to us with symptoms of dysphagia, hoarseness of voice, and exertional dyspnea.
Aniket Puri +5 more
openaire +3 more sources
Abnormality Detection and Localization in Chest X-Rays using Deep Convolutional Neural Networks [PDF]
arXiv, 2017 Chest X-Rays (CXRs) are widely used for diagnosing abnormalities in the heart and lung area. Automatically detecting these abnormalities with high accuracy could greatly enhance real world diagnosis processes. Lack of standard publicly available dataset and benchmark studies, however, makes it difficult to compare various detection methods. In order to
arxiv
The Pan African Medical Journal, 2017 Introduction The cardio-thoracic ratio (CTR) and the transverse cardiac diameter (TCD) on Plain chest radiography are the two parameters commonly used to diagnose cardiomegaly and heart disease.
E. Brakohiapa +4 more
semanticscholar +1 more source
International Journal of Gynecology &Obstetrics, Volume 169, Issue 2, Page 623-629, May 2025.Abstract Objective Prior to 2019, termination of pregnancy (TOP) was unlawful in Ireland. We sought to examine the impact of legislative change on TOP for major congenital heart disease (CHD) and its effect on parental decision‐making regarding the options of complex surgery, TOP, or palliative perinatal care.
Fiona Cody +7 more
wiley +1 more source
The caveats in the diagnosis of anomalous origin of left coronary artery from pulmonary artery (ALCAPA) [PDF]
, 2010 Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is an infrequent, well described, but important anomaly of the coronary origin. Early diagnosis and prompt surgical treatment of the disease can be life saving. However, there are
Kothari, Shyam S., Varghese, M.J.
core +1 more source
International Journal of Gynecology &Obstetrics, Volume 169, Issue 2, Page 474-484, May 2025.Abstract The ex‐utero intrapartum treatment (EXIT) procedure is a specialized delivery strategy that extends utero–placental–fetal circulation to convert a potential neonatal emergency condition into a condition that is compatible with postnatal life. Cesarean section with operation on placental support is an EXIT technique that requires a relatively ...
Sanpon Diawtipsukon +3 more
wiley +1 more source
Association of Cystic Medial Necrosis of the Aorta and Undiagnosed Thyroiditis [Scripta Medica] [PDF]
, 1977 We have recently seen two patients with cystic medial necrosis of the aorta. The first patient died of a dissecting aneurysm of the thoracic aorta. At autopsy, classical Hashimoto’s thyroiditis was discovered.
Hain, John R., Wise, William S.
core +1 more source
Unsupervised Domain Adaptation for Automatic Estimation of Cardiothoracic Ratio [PDF]
arXiv, 2018 The cardiothoracic ratio (CTR), a clinical metric of heart size in chest X-rays (CXRs), is a key indicator of cardiomegaly. Manual measurement of CTR is time-consuming and can be affected by human subjectivity, making it desirable to design computer-aided systems that assist clinicians in the diagnosis process.
arxiv