Congenital mydriasis as an initial sign of septo-optic dysplasia

Septo-optic dysplasia (SOD)[MIM182230] consisting of a heterogeneous and uncommon condition characterised by the classictriad: optic nerve hypoplasia, abnormalities of pituitary hormone, and defects of thebrain midline (including agenesis of the septum pellucidum and/or the corpus callosum; ithas al...

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Veröffentlicht in:Archivos de la Sociedad Española de Oftalmología 2013-10, Vol.88 (10), p.398-402
Hauptverfasser: Carrascosa-Romero, M C, Ruiz-Cano, R, Martínez-López, F, Alfaro-Ponce, B, Pérez-Pardo, A
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Sprache:spa
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Zusammenfassung:Septo-optic dysplasia (SOD)[MIM182230] consisting of a heterogeneous and uncommon condition characterised by the classictriad: optic nerve hypoplasia, abnormalities of pituitary hormone, and defects of thebrain midline (including agenesis of the septum pellucidum and/or the corpus callosum; ithas also been described associated cortical malformations, it was referred to as SOD plus syndrome).We report the first known case in which the initial diagnostic sign of SOD was a bilateralmydriasis as a manifestation ofhypoplasia of both optic nerves, pituitary hypoplasia andcerebral dysgenesis with neuronal migration disorder.We discuss thedifferential diagnosis of congenital mydriasis.
ISSN:1989-7286
DOI:10.1016/j.oftal.2012.05.005