Searchable abstracts of presentations at key conferences in endocrinology

ea0063p475 | Calcium and Bone 2 | ECE2019

McCune-Albright syndrome: report of two cases

Kalantzi Athanasia , Giagourta Eirini , Tournis Simeon , Papanastasiou Labrini , Gravvanis Christos , Glykofrydi Spyridoula , Chantziara Maria , Theodoropoulou Georgia , Patikos Christos , Georgakoulias Nikolaos , Kounadi Theodora

Introduction: McCune-Albright syndrome (MAS) is a rare non-inheritable genetic disease. It is attributed to an early embryonic postzygotic somatic activating mutation of GNAS, leading to a mosaic that causes polyostotic fibrous dysplasia, café au lait macules and polyendocrinopathy.Aim: To present two cases of this rare syndrome.Case report: A 38-year-old male patient presented with a bone lesion of the forehead and acromegali...