Prader–Willi syndrome in neonates: twenty cases and review of the literature in Southern China

@inproceedings{Wang2016PraderWilliSI,
  title={Prader–Willi syndrome in neonates: twenty cases and review of the literature in Southern China},
  author={Ping F. Wang and Wei Zhou and Weiming Yuan and Longguang Huang and Ning Zhao and Xiaowen Chen},
  booktitle={BMC pediatrics},
  year={2016}
}
BACKGROUND Prader-Willi syndrome is a rare genetic abnormality that can be challenging to diagnose early, but for which early interventions improve prognosis. METHODS To improve understanding of Prader-Willi syndrome in neonates in Asia, we retrospectively analyzed the clinical records of 20 affected newborns diagnosed in the Department of Neonatology… CONTINUE READING