New Discovery Suggests Deficiency in PC1 May Cause Many Symptoms of PWS
Foundation For Prader-Willi Research
Published at : 09 Dec 2020
FPWR funded researchers, Drs. Burnett and Leibel, have published a breakthrough discovery that could change our understanding of PWS and open up new avenues for therapeutic development. Now that we have a possible explanation for the wide array of symptoms, we may be able to develop a drug that addresses the underlying cause, instead of treating each symptom individually.