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Home Our Mission The Disease Research Blog Donate Latest News These beautiful children are suffering from a rare disease caused by loss of function of the FAM177A1 gene. Disruptions of the FAM177A1 gene cause intellectual disability seizures autism progressive motor decline and other debilitating issues. There are currently no diseasespecific treatments. The FAM177A1 Research Fund is a familyled patient advocacy organization dedicated to improving the lives of everyone impacted by FAM177A1related Neurodevelopmental Disorder.