Discovery of a Novel Ultra-Rare Hereditary Ataxia Syndrome Caused by Changes in the POU4F1 Gene
November 7, 2025
Written by: Sophia Salemi, BSÂ Edited by: Celeste Suart, PhDÂ Article highlight: Scientists have discovered that changes in the POU4F1 gene can cause a very rare hereditary ataxia syndrome with first symptoms beginning in childhood. A new patient registry is now open, giving families the opportunity to join a growing community Read More…
