Results 31 to 40 of about 316,820 (154)

Associations between the Severity of the Post-Acute COVID-19 Syndrome and Echocardiographic Abnormalities in Previously Healthy Outpatients Following Infection with SARS-CoV-2

Biology, 2021
The COVID-19 pandemic affected over 130 million individuals during more than one year. Due to the overload of health-care services, a great number of people were treated as outpatients, many of them subsequently developing post-acute COVID-19 syndrome ...
Cristina Tudoran, Mariana Tudoran, Gheorghe Nicusor Pop, Catalina Giurgi-Oncu, Talida Georgiana Cut, Voichita Elena Lazureanu, Cristian Oancea, Florina Parv, Tudor Ciocarlie, Felix Bende   +9 more
doaj   +1 more source

The right coronary artery originating from the distal circumflex artery [PDF]

Ķazaķstannyṇ Klinikalyķ Medicinasy, 2019
We report a case of anomalous origin of the right coronary artery in a 58-year-old male patient. The patient had a single coronary ostium originating from the left sinus valsalva.
Songül Cuglan, Bilal Cuglan
doaj   +1 more source

Combination between Dunbar Syndrome and May–Thurner syndrome: A rare case Report

Journal of Medical Ultrasound, 2023
Dunbar syndrome (DS) and May–Thurner syndrome (MTS) are part of a group of rare vascular disorders known as “vascular compression syndromes.” Dunbar's syndrome is caused by the median arcuate ligament of diaphragm, which, due to an abnormal course ...
Renato Farina, Federica Galioto, Davide Castiglione, Antonio Basile   +3 more
doaj   +1 more source

Coronary Myocardial Bridge Updates: Anatomy, Pathophysiology, Clinical Manifestations, Diagnosis, and Treatment Options [PDF]

Texas Heart Institute Journal
Myocardial bridging is a frequent anomaly of the heart in humans and other animals. A myocardial bridge is typically characterized by the systolic narrowing seen with traditional catheter angiography, but this abnormality is not by itself a sign of ...
Paolo Angelini, MD, Carlo Uribe, MD, Arjun Raghuram   +2 more
doaj   +1 more source

HFpEF: Cardiovascular Abnormalities Not Just Comorbidities [PDF]

Circulation: Heart Failure, 2012
Twenty-five years ago, the understanding of heart failure (HF) was straightforward. HF was a clinical syndrome due to left ventricular (LV) systolic dysfunction apparent as a reduced ejection fraction (EF). Based on this understanding, large randomized trials were conducted using an EF0.50, an EF that is in the normal or near-normal range (ie ...
William C, Little, Michael R, Zile
openaire   +2 more sources

Modifying influence of subclinical hypothyroidism on arterial hypertension: relationship to masked treatment failure, circadian blood pressure profile and target organs status

Клиническая и экспериментальная тиреоидология, 2015
Aim. The study aimed to investigate the modifying influence of subclinical hypothyroidism (SH) on arterial hypertension (AH), the prevalence of masked uncontrolled hypertension, circadian blood pressure (BP) profile and cardiovascular disorders ...
T A Nekrasova, L G Strongin, E P Morozova, E M Durigina, L V Kasakova   +4 more
doaj   +1 more source

Dental considerations and management in Noonan Syndrome: A case report with review of literature

Contemporary Pediatric Dentistry, 2021
Noonan syndrome is a genetic disorder of autosomal dominance with an estimated prevalence of 1:1000 – 1:2500 live birth. The typical features include short stature, cardiovascular abnormalities and characteristics facial deformity.
Nipun Jain, Priyanka Venugopal, Arun Mamachan Xavier, Parvathy Kumaran, Balagopal R Varma, Suresh Kumar J   +5 more
doaj   +1 more source

Risk of sudden cardiac death and preventive measures in athletes

International Journal of the Cardiovascular Academy, 2022
Arrhythmias, which are fatal in some patients, can be triggered by sports in vulnerable people. It is estimated that 1:40,000–1:250,000 athletes will suffer a sudden cardiac death (SCD).
Adel Khalifa Sultan Hamad
doaj   +1 more source

Craniofacial and Oral Features of Williams Syndrome- A Rare Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2020
Williams syndrome is a rare genetic disorder that occurs due to deletion on chromosome 7q11.23. The prevalence is said to be 1:7500-1:20,000. The typical presentation of the syndrome includes dysmorphic facial features, cardiovascular malformations and
G Geethanjali, Amarshree A Shetty, Amitha M Hegde   +2 more
doaj   +1 more source

Idiopathic dilatation of the pulmonary artery: a pediatric case report and literature review

Frontiers in Cardiovascular Medicine
BackgroundIdiopathic dilatation of the pulmonary artery (IDPA) is a rare vascular anomaly characterized by isolated dilation of the main pulmonary artery.
Jingwei Sun, Jiachen Li, Mengjing Wang, Nan Dong, Dong Qi   +4 more
doaj   +1 more source