Recent scientific advancements in cancer research are unveiling the complex behaviors and interactions within tumors through innovative technologies such as 3D tumor mapping and single-cell analysis. These methods allow researchers to delve deeper into the intricacies of tumor development and
Congenital heart disease (CHD) is a significant cause of infant morbidity and mortality, characterized by structural abnormalities in the heart or great vessels present at birth. This article delves into the clinical features, genetic characteristics, and pregnancy outcomes of 471 cases of fetal
Rare diseases, though individually uncommon, collectively impact millions of people worldwide. Most of these conditions manifest in childhood, with genetic factors being the primary cause in about 80% of cases. Children with rare genetic disorders often endure prolonged diagnostic journeys
The world of viral genomics has long been defined by the minimalist nature of most viral genomes, containing only the essential genes required for survival, as viruses tend to shed any genes that don’t confer a clear advantage. However, the SARS-CoV-2 virus, responsible for the global COVID-19 p
Recent research, published in the Journal of Translational Internal Medicine, delves into the intriguing association between gastroesophageal reflux disease (GERD) and cardiovascular health. GERD, primarily recognized as a digestive disorder characterized by acid reflux and heartburn, has now been
Polycystic Ovary Syndrome (PCOS) is a common hormonal disorder affecting women of reproductive age. Characterized by symptoms such as irregular menstrual cycles, excessive androgen levels, and ovarian cysts, PCOS is also associated with significant metabolic complications like insulin resistance,
