On June 11, 2025, a lecture titled "What Do We Know About Alpha-Mannosidosis?" was held in Taldykorgan as part of a master class on rare diseases in pediatric neurology.

Alpha-mannosidosis is a rare inherited metabolic disorder. The presentation covered key clinical features, diagnostic challenges, and approaches to differential diagnosis.

Special emphasis was placed on the importance of early detection and the need for greater awareness among primary care physicians. Timely referral for biochemical and genetic testing can significantly improve outcomes and quality of life for patients.

The topic sparked strong interest and active discussion among medical professionals, highlighting the need for knowledge sharing and a multidisciplinary approach in managing rare diseases!