Volodymyr S Andrukh*
Children's Hospital, Dolyna, Ukraine
*Corresponding Author: Volodymyr S Andrukh, Children's Hospital, Dolyna, Ukraine.
Received: February 24, 2020; Published: March 04, 2020
We present a clinical pattern of Prader-Labhart-Willi syndrome in a 16-month-old boy. The syndrome is characterized by the development of severe obesity and delayed psychomotor and sexual development as well as a determined dysfunction of the РWS-АS site in the 15th pair of chromosomes of male origin. The peculiarity of the case is apnea manifestations, which are likely to lead to fatal outcome.
Keywords: Prader-Labhart-Willi; Syndrome; Children
Citation: Volodymyr S Andrukh. “Prader-Labhart-Willi Syndrome”. Acta Scientific Paediatrics 3.4 (2020): 22-23.
Copyright: © 2020 Volodymyr S Andrukh.This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.