We report a case of pituitary duplication in a neonate girl whose magnetic resonance (MR) images showed unusual findings of hypogenesis of the corpus callosum and oral dermoid. Pituitary duplication is an extremely rare malformation, with only a few previously reported cases. It occurs most commonly in association with complicated midline and skull base anomalies. We present a case of this malformation with special emphasis on the hypogenesis of splenium of the corpus callosum and oral dermoid. © Springer-Verlag 2004.
CITATION STYLE
Mutlu, H., Paker, B., Gunes, N., Emektar, A., Keceli, M., & Kantarci, M. (2004). Pituitary duplication associated with oral dermoid and corpus callosum hypogenesis. Neuroradiology, 46(12), 1036–1038. https://doi.org/10.1007/s00234-004-1296-x
Mendeley helps you to discover research relevant for your work.