Fragile X syndrome (FXS) is the leading monogenetic cause of cognitive impairment and autism spectrum disorder. Area CA1 of the hippocampus receives current information about the external world from the entorhinal cortex via the temporoammonic (TA) pathway. Given its role in learning and memory, it is surprising that little is known about TA long-term potentiation (TA-LTP) in FXS. We found that TA-LTP was impaired in male fmr1 KO mice. Although there were no significant differences in basal synaptic transmission, synaptically evoked dendritic calcium signals were smaller in KO neurons. Using dendritic recording, we found no difference in complex spikes or pharmacologically isolated Ca2+ spikes; however, the threshold for fast, Na+ dependent dendritic spikes was depolarized in fmr1 KO mice. Cell-attached patch clamp recordings found no difference in Na+ channels between wild type and fmr1 KO CA1 dendrites. Dendritic spike threshold and TA-LTP were restored by block of A-type K+ channels with either 150 μM B...