This website provides information on patients with mutations in the METTL23 gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the METTL23 gene is an autosomal recessive disorder characterized by intellectual disability (ID) and variable dysmorphic features

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the METTL23 gene.

Mohammed Almannai, MD, Genetics and Precision Medicine Department, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia, almannaimo@mngha.med.sa