MeSH tree: C16.320
A team from the Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), working with a large international network of hospitals and research centers, has shown that left ventricular hypertrabeculation—an anatomical ...
Aug 5, 2026
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Children born with a pathogenic variant in the TP53 gene, known as Li-Fraumeni syndrome, have a markedly increased risk of developing various types of cancer, often at a young age. Therefore, they undergo regular surveillance ...
Aug 5, 2026
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An analysis in JDDG: Journal der Deutschen Dermatologischen Gesellschaft found that people with eczema (also known as atopic dermatitis) face an elevated risk of developing shingles (or herpes zoster).
Aug 5, 2026
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A new study co-led by professor Valeriya Malysheva, group leader at the VIB-UAntwerp Center for Molecular Neurology, published in Nature Genetics, uncovers how the three-dimensional organization of DNA in rare immune cells ...
Aug 4, 2026
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Teeth and bones are among the hardest structures in the human body, but certain inherited conditions can rob them of that strength. One of them is hypophosphatasia (HPP), a rare, lifelong genetic bone disorder that disrupts ...
Lung infections are a constant risk for people living with cystic fibrosis (CF), a life-threatening genetic disorder that impairs lung function, predisposes people to persistent airway infections and puts them at risk of ...
Aug 3, 2026
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A pair of wearable stickers may transform diagnostic sweat testing for cystic fibrosis (CF), a genetic disorder that causes problems with digestion and breathing.
Aug 1, 2026
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A protein best known for protecting the ends of chromosomes also helps muscle stem cells preserve their identity and repair damaged tissue, according to a new study from researchers at the Perelman School of Medicine at the ...
Jul 31, 2026
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Lysosomes, the cell's recycling hubs, are best known for their role in a group of rare inherited conditions called lysosomal storage disorders, where harmful molecules build up inside these compartments. But scientists are ...
Jul 31, 2026
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In a study published in the journal Science, researchers in Queensland and the United States discovered that the human X chromosome attracts an unusual kind of DNA mutation, potentially doubling the risk of certain genetic ...
Jul 31, 2026
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