We review the systematics of frogs of the Hyloscirtus larinopygion group. A new phylogenetic tree inferred from mitochondrial DNA (partial sequences of 12S rRNA, valine-tRNA, and 16S rRNA genes; ∼2.3 kb) of eleven species of the H. larinopygion group is provided, based on maximum parsimony, maximum likelihood, and Bayesian analyses. Our phylogeny confirms the close relationship of members of the H. larinopygion group with Andean relatives of the H. armatus group, which also occurs in the Andes. Hyloscirtus tapichalaca is placed as sister species to the rest of the H. larinopygion group, in which two clades (A+B) are evident. Although ingroup relationships are well supported, the monophyly of the H. larinopygion group and placement of H. tapichalaca require additional testing. Genetic divergences among species of the H. larinopygion group are shallow compared to those observed in many other anurans, with genetic distance among sister species (H. princecharlesi and H. ptychodactylus) as low as 1.31%. However, this pattern is concordant with radiations in other highland Andean lineages of anurans that show marked morphological or behavioral differentiation, but low divergence in mitochondrial markers. Divergence-time analyses (using BEAST) indicate that the Hyloscirtus clade is a relatively ancient lineage that appeared in the Eocene, at a minimum age of 51.2 million years ago (MYA), while the H. larinopygion group originated in the Middle-Late Eocene at a minimum age of 40.9 MYA. Our results might suggest a rapid radiation of Hyloscirtus starting in the Miocene into the Pliocene, from at least 14.2 MYA to the most recent divergence between sister taxa at ∼2.6 MYA. We also describe two sympatric new species of Hyloscirtus from northwestern Ecuador: H. criptico sp. nov. and H. princecharlesi sp. nov. We diagnose them by their phylogenetic position (they are not sister to each other), genetic divergence, and a unique combination of color patterns, and other morphological features. Additionally, we describe the suctorial tadpoles and the extreme ontogenic color changes in H. larinopygion, H. lindae, H. pantostictus, H. princecharlesi, H. psarolaimus, and H. tigrinus. Furthermore, we describe the osteology of H. criptico, H. lindae, H. pacha, H. pantostictus, H. princecharlesi, H. psarolaimus, H. ptychodactylus, and H. staufferorum. We describe vocalizations of H. lindae, H. pacha, H. pantostictus, H. pasarolaimus, H. staufferorum, and H. tapichalaca. Hyloscirtus tigrinus is recorded for the first time in Ecuador and its range is extended 62.4 km (airline distance), from its southernmost locality record in Departamento de Nariño, Colombia. Most species of the H. larinopygion group are currently severely threatened by extinction, after surviving the catastrophic extinctions in the 1980s and 1990s that led to the disappearance of many other sympatric anurans that bred in swiftly flowing water and had lotic water tadpoles in the Andean highlands. Research and conservation actions are urgently needed for these species. In order to better call attention to these conservation issues, we name one of the new species in honor of Prince Charles of Wa l e s, who is contributing significantly to the growth of awareness in the battle against tropical deforestation, climate change, and the catastrophic extinction of rainforest amphibians.