hrp0098p2-369 | Late Breaking | ESPE2024

Management challenges of an infant with multiple endocrinopathies with McCune Albright Syndrome: A Case Report

Wijalathgedera Oshan , Damayanthi Liyanage Lasika , Suntharesan Jananie

Introduction: McCune Albright syndrome (MAS) is a rare genetic disorder characterized by a triad of hyperpigmentation, endocrinopathies, and fibrous dysplasia (FD), caused by post-zygotic somatic mutations. Hyperthyroidism is the second most common endocrinopathy in MAS and poses significant management challenges in infants.Case History: 7-month-old infant girl born to non-consanguineous parents, who presented with per v...