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Gene Mutation
🚨 please share for awareness 🚨 CTNNB1 syndrome, also known as beta-catenin-related intellectual disability syndrome, is a rare genetic disorder caused by mutations in the CTNNB1 gene. This gene encodes beta-catenin, a protein that plays a crucial role in cell signaling, gene transcription, and cell adhesion. Mutations in this gene can lead to a range of developmental and health issues. Key Features and Symptoms The symptoms and severity of CTNNB1 syndrome can vary, but common features…
