Child with rare genetic syndrome successfully treated in less than two years
EAST LANSING, Mich. - Diagnosing a rare medical condition is difficult. Identifying a treatment for it can take years of trial and error. In a serendipitous intersection of research expertise, an ill patient in this case a child and innovative technology, Bachmann-Bupp Syndrome has gone from a list of symptoms to a successful treatment in just 16 months.
The paper chronicling this lightning-fast scientific response to the Bachmann-Bupp Syndrome was published in the open-access journal, eLife.
For more than 25 years, André Bachmann, professor of pediatrics in Michigan State University College ...











