MeSH tree: C16.131.240.400
Babies born prematurely can have a number of complications at birth, simply because they are brought into the world before their organs are fully developed. One complication is called patent ductus arteriosus (PDA).
Dec 9, 2025
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A new national analysis shows that over the past two decades, inpatient care for children with complex chronic conditions (CCCs) has become far more intensive—and is now overwhelmingly concentrated in urban teaching children's ...
Dec 2, 2025
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Scanning for serious structural issues in fetuses during the first trimester can result in earlier detection of these issues, reports a new study led by Aris Papageorghiou at the University of Oxford, United Kingdom, published ...
Nov 25, 2025
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At Mayo Clinic, cardiologists Peter Noseworthy, M.D., and John Giudicessi, M.D., Ph.D., are uncovering the earliest signs of a genetic heart condition that often strikes without warning. Their work shows that early detection, ...
Nov 11, 2025
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For decades, it was impossible for clinicians to know which babies with major heart defects might eventually have developmental abnormalities, like ADHD and learning differences. Now, by adapting a simple and safe oxygen ...
Nov 10, 2025
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In cases of mild congenital heart defects, more prenatal visits are associated with a greater likelihood of appropriate delivery at a community hospital, according to a study published in JAMA Network Open. Results suggest ...
Nov 9, 2025
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The Society for Cardiovascular Angiography & Interventions (SCAI) has published a comprehensive roadmap that details the use of intracardiac echocardiography (ICE) to guide structural heart disease (SHD) interventions for ...
Oct 7, 2025
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Researchers from the University of Copenhagen have developed a method that allows for the analysis of thousands of proteins in heart tissue. This provides entirely new insights into the characteristics of heart diseases and ...
Oct 2, 2025
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The U.S. Food and Drug Administration has granted accelerated approval to Forzinity (elamipretide) injection as the first treatment for Barth syndrome.
Sep 25, 2025
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Noonan syndrome with multiple lentigines (NSML) is a rare genetic disorder that causes short stature, distinctive facial features, and clusters of dark skin spots called lentigines. But its most serious impact is a dangerous ...
Sep 16, 2025
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