hrp0098p3-45 | Bone, Growth Plate and Mineral Metabolism | ESPE2024

A case report of rare McCune-Albright Syndrome

Bolatbek Kassiyet , Rakhimzhanova Marzhan , Ermukenova Madina

Introduction: McCune Albright syndrome (MAS) is a rare disease caused by mutations of the GNAS1 gene, clinically it is characterized by the classic triad of polyostotic fibrous dysplasia (POFD), cafe-au-lait skin pigmentation, and peripheral precocious puberty.Case Report: We present a clinical case of an 8-year-old boy with a cafe-au-lait skin pigmentation diagnosed with McCune-Albright syndrome in the Republic of Kazak...