Revista nº 816

Displasia septo-óptica/síndrome de Morsier | Sánchez Mellado A, et al. 120 Actual Med.2022;107(816):117- 120 4. Revista Española Endocrinología Pediátrica - Displasia sep- to-óptica de presentación neonatal. https://www.endocri- nologiapediatrica.org/modules.php?name=articulos&idar- ticulo=88&idlangart=ES. Accessed May 4, 2021. 5. Dattani MT, Martinez-Barbera JP, Thomas PQ, et al. Muta- tions in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse. Nat Genet. 1998;19(2):125-133. doi :10.1038/477 6. Kelberman D, De Castro SCP, Huang S, et al. SOX2 plays a critical role in the pituitary, forebrain, and eye during hu- man embryonic development. J Clin Endocrinol Metab. 2008;93(5):1865-1873. doi :10.1210/jc.2007-2337 7. Signorini SG, Decio A, Fedeli C, et al. Septo-optic dys- plasia in childhood: The neurological, cognitive and neuro-ophthalmological perspective. Dev Med Child Neurol. 2012;54(11):1018-1024. doi: 10.1111/j.1469- 8749.2012.04404.x 8. Ward DJ, Connolly DJA, Griffiths PD. Review of the MRI brain findings of septo-optic dysplasia. Clin Radiol. 2021;76(2):160.e1-160.e14. doi :10.1016/j.crad.2020.09.007 Si desea citar nuestro artículo: Sánchez Mellado A, Montoro Moreno R, Lacorzana J. Displasia septo-óptica/síndrome de Morsier;una enfermedad que sos- pechar. Actual Med.2022;107(816):117- 120. DOI:10.15568/ am.2022.816. cc01