Magonjwa
Researchers identify rare NAMPT-linked disorder known as MINA syndrome
Imeripotiwa na AI Picha iliyoundwa na AI Imethibitishwa ukweli
An international team led by Shinghua Ding at the University of Missouri has identified a rare genetic disorder called Mutation in NAMPT Axonopathy (MINA) syndrome, tied to a mutation in the NAMPT protein that undermines energy production in nerve cells and impairs motor function.
Maafisa wa afya wameingia katika hali ya tahadhari baada ya kuthibitishwa kisa kimoja cha ugonjwa wa Homa ya nyani katika Kaunti ya Embu.
Imeripotiwa na AI
Moderna confirmed ongoing work on an mRNA vaccine for hantavirus following a deadly outbreak on a Dutch cruise ship. The effort, in partnership with Korea University, began in 2023 and shows promise but remains years from completion.