hrp0097p1-488 | Fetal, Neonatal Endocrinology and Metabolism | ESPE2023
Prylutskaya Veranika
, Trebka Ekaterina
, Solntsava Anzhalika
, Naumchik Irina
, Demidovich Tatjana
Background and aim: Prader-Willi Syndrome (PWS) is a rare disease with various clinical signs in different age periods. Early diagnosis has a proven benefit in PWS, allows for timely diet therapy and prevention of obesity, early administration of growth hormone. The purpose of the study is to analyze the features of neonatal adaptation in children with PWS, to evaluate the diagnostic efficacy in the dynamics of the analyzed period.<stron...