Illustration of scientists in a lab discovering MINA syndrome, a rare genetic disorder affecting nerve cells and motor function.
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Researchers identify rare NAMPT-linked disorder known as MINA syndrome

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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.

Health officials are on high alert after one case of mpox was confirmed in Embu County.

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