Literature DB >> 24060304

[Congenital mydriasis as an initial sign of septo-optic dysplasia].

M C Carrascosa-Romero1, R Ruiz-Cano, F Martínez-López, B Alfaro-Ponce, A Pérez-Pardo.   

Abstract

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.
Copyright © 2010 Sociedad Española de Oftalmología. Published by Elsevier Espana. All rights reserved.

Entities:  

Keywords:  Agenesia septum pellucidum; Agenesis septum pellucidum; Alteración migración neuronal; Amaurosis; Congenital mydriasis; Displasia septo-óptica; Hipoplasia nervio óptico; Impaired neuronal migration; Midriasis; Midriasis congénita; Morsier syndrome; Mydriasis; Optic nerve hypoplasia; Septo-optic dysplasia; Síndrome de Morsier

Mesh:

Year:  2012        PMID: 24060304     DOI: 10.1016/j.oftal.2012.05.005

Source DB:  PubMed          Journal:  Arch Soc Esp Oftalmol        ISSN: 0365-6691


  1 in total

1.  Bilateral congenital mydriasis in a child case.

Authors:  Bengi Ece Kurtul; Pınar Altıaylık Özer; Ayla Akca Çağlar; Emrah Utku Kabataş
Journal:  Turk Pediatri Ars       Date:  2016-09-01
  1 in total

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