Familial Mediterranean fever is an autosomal recessive genetic disorder characterized by recurrent febrile polyserositis, especially prevalent in individuals of Mediterranean descent. Familial ...

Using a mouse model for familial Alzheimer's disease, the addition of craniosynostosis and associated impairments to the lymphatic and glymphatic systems caused a significant increase in plaque ...

FGF23 is broadly implicated in human disease, including autosomal-dominant hypophosphataemic rickets, tumour-induced osteomalacia, familial tumoral calcinosis and end-stage kidney disease.