hrp0084p2-500 | Perinatal | ESPE2015
, Diene Gwenaelle
, Molinas Catherine
, Casper Charlotte
, Tauber Maithe
Background: Prader-Willi syndrome (PWS) is a rare and complex genetic disorder characterised in neonates by hypotonia and feeding problems. French birth incidence has never been reported.Objective and hypotheses: To evaluate incidence of PWS at birth in France.Method: Identification of patients with a molecular diagnosis of PWS born between January 1st, 2013 and December 31st, 2013 was obtained by combining va...