In the third in his special series of articles exploring the enduring legacy of Tutankhamun, Zahi Hawass searches for the boy king’s relatives among mummies thought to belong to the royal family ...

Researchers working on an incurable blood cancer can now use a new lab model that could make testing potential new treatments and diagnostics easier and quicker, new research has found.

Donations will go towards Immie and her family making memories together and the living costs that come with caring for a ...

OMRF researchers uncover a genetic link between lymphatic valve formation and Crohn's disease, paving the way for future treatments.

Eggs and embryos from people with polycystic ovary syndrome have altered patterns of so-called epigenetic tags, which could ...

Nicolina was diagnosed with Marfan's Syndrome and a rare genetic disorder, leading to persistent complications including a ...

MS is a genetic disorder first identified in 1896 by the French pediatrician Antoine Bernard Marfan. It shows significant phenotypic variability, with mild-to-severe and potentially fatal cases. 2 The ...

Osteogenesis imperfecta, Ehlers-Danlos syndrome, and Marfan syndrome form a group of genetic disorders of connective tissue. These disorders exhibit remarkable clinical heterogeneity which reflects ...

Marfan syndrome (MFS) is a systemic heritable connective tissue disorder caused by pathogenic variants in the FBN1 gene. Previous studies have documented the clinical utility of FBN1 mutation ...