DEVELOPMENTAL NEUROSCIENCEReduced basal forebrain and hippocampal activation during memory encoding in girls with fragile X syndromeGreicius, Michael D.1 2; Boyett-Anderson, Jesse M.2; Menon, Vinod2 3 4; Reiss, Allan L.2 3 4 CAAuthor Information Departments of 1Neurology and Neurological Sciences 2Psychiatry and Behavioral Sciences 3Program in Neuroscience 4Stanford Brain Research Institute, Stanford University School of Medicine, Stanford, CA 94305, USA CACorresponding Author: email@example.com Received 5 April 2004; accepted 15 April 2004 NeuroReport: July 19th, 2004 - Volume 15 - Issue 10 - p 1579-1583 doi: 10.1097/01.wnr.0000134472.44362.be Buy SDC Metrics Abstract Fragile X syndrome (FraX), the most common heritable cause of developmental disability, is associated with IQ, memory, and visuospatial processing deficits. The fragile X gene (FMR1) is prominently transcribed in two regions critical to memory encoding and attention: the hippocampus and the basal forebrain. To probe functional MRI activation abnormalities associated with the disorder, girls with FraX and age-matched, normally-developing girls were scanned during a test of visual memory encoding. While there were considerable similarities in activation patterns between the two groups, the girls with FraX showed significantly less activation in the hippocampus and the basal forebrain. This is the first study, to our knowledge, demonstrating functional deficits in FraX subjects in brain regions known to have the highest FMR1 transcription. © 2004 Lippincott Williams & Wilkins, Inc.