ea0035p853 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014
Grugni Graziano
, Corrias Andrea
, Sartorio Alessandro
, Beccaria Luciano
, Bocchini Sarah
, Di Candia Stefania
, Fintini Danilo
, Iughetti Lorenzo
, Mussa Alessandro
, Ragusa Letizia
, Gargantini Luigi
, Salvatoni Alessandro
, Delvecchio Maurizio
, Chiumello Giuseppe
, Crino Antonino
Introduction: Hypothalamicpituitary anomalies are well proven in PraderWilli syndrome (PWS). In this context, it has been previously reported that central adrenal insufficiency (CAI) may be part of the PWS phenotype. However, the diagnostics of CAI is critical and debated, due to the lack of fully reliable tests. Several studies have looked at the clinical usefulness of the low dose (1 μg) short Synacthen test (LDSST) compared to the conventional dose (250 	...