Ontogenetic changes in the brain and sensory systems play an essential role in shaping behavioral performance and ecological specialization in vertebrates; however, these developmental pathways are inadequately recorded in endangered crocodylians. Here, we present the first quantitative analysis of endocast and endosseous labyrinth development across ontogeny in the Siamese freshwater crocodile (Crocodylus siamensis), a critically endangered species from Southeast Asia. Using high-resolution computed tomography (CT) and three-dimensional reconstruction, we examined six skulls representing juvenile, subadult, and adult growth stages. Our findings reveal a consistent pattern of allometric scaling, correlated with marked morphological changes in sensory-related neuroanatomical structures. Juveniles display strongly curved forebrains and proportionally prominent olfactory regions, which is in line with their early reliance on chemosensory cues. As skull size increases, the encephalic endocast becomes longer and straighter, while regions corresponding to the midbrain and hindbrain show proportional morphological changes associated with visual processing and motor coordination, suggesting ontogenetic changes in regions associated with visual processing and motor coordination. Parallel ontogenetic transformations are also observed in the endosseous labyrinth, including increased lagena dimensions and more pronounced semicircular canal curvature in adults. These changes are consistent with ontogenetic variation in structures associated with auditory and vestibular functions. Strong correlations between dorsal cranial length and both endocast and labyrinthine parameters suggest that sensory-related neuroanatomical morphology in C. siamensis follows a consistent ontogenetic scaling pattern. These findings establish an important neuroanatomical baseline for understanding sensory ecology in this endangered crocodilian and provide a comparative framework for interpreting fossil crocodylian neuroanatomy, with implications for conservation biology, functional morphology, and paleoneurology.


