ea0063p475 | Calcium and Bone 2 | ECE2019
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...