KNOXVILLE -- Findings reported in this month's issue of PLoS Biology give insight into the unique characteristics of the birth defect known as Prader-Willi Syndrome (PWS), and at the same time, may help explain the way that a certain type of gene is expressed in all humans.
The research by University of Tennessee, Knoxville, professor Francisco Ubeda finds that the amount of care a father gives to his child may cause a shift in the syndrome in which its symptoms, in essence, reverse themselves.