Complicanze endocrine nelle malattie metaboliche ereditarie

Classic galactosemia is a rare inherited metabolic disorder that requires early diagnosis and lifelong multidisciplinary management. This webinar will explore the clinical journey of patients with classic galactosemia, from neonatal diagnosis through to the main endocrine complications, with a particular focus on pubertal development and ovarian function. The aim is to provide an integrated metabolic and endocrinological overview of classic galactosemia, promoting a shared approach to diagnosis, monitoring, and patient management.