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Hace 5 días · Spontaneous coronary artery dissection (SCAD) is an increasingly recognised cause of acute coronary syndrome (ACS) in younger women. SCAD was first described in the British Medical Journal in 1931 ...
Hace 18 horas · Background A person with epilepsy experiences recurrent seizures as a result of a persistent underlying disorder. About 50 million people globally are impacted by it, with 4 million of those being in Sub-Saharan Africa. One of the most frequent comorbidities that raise the mortality and morbidity rates of epileptic patients is abnormal Electrocardiographic (ECG) findings. Thus, the purpose of ...
Hace 1 día · Quadricuspid aortic valve (QAV) is a rare congenital anomaly with <200 cases reported to date. Most patients are asymptomatic. ... The patient was kept on close medical follow-up. Note: *, aortic leaflets; RA, right atrium; LA, left atrium; RV, right ventricle; LV, left ventricle; VSD, ventricular septal defect; RVOT, right ...
Hace 18 horas · A multi-institutional team of archaeological researchers from Japan and Egypt has discovered what they describe as an underground "anomaly" near the iconic Giza pyramid complex. In their study ...
Hace 2 días · Sickle cell disease ( SCD ), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. [2] . The most common type is known as sickle cell anemia. [2] . It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [2] .
Hace 5 días · Breast cancer is the most frequently diagnosed malignancy (barring skin cancers) and the fifth leading cause of cancer-related deaths worldwide [1, 2].According to GLOBOCAN 2022, 2.3 million new cases of breast cancer were diagnosed in 2022, with 666,103 patients dying from the disease [].Moreover, the incidence and mortality of breast cancer is expected to increase by 40% and 50% respectively ...
Hace 3 días · Down syndrome. Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [3] It is usually associated with developmental delays, mild to moderate intellectual disability, and characteristic physical features.
