Literature DB >> 9606688

[Septo-optic dysplasia (de Morsier syndrome)].

M Stangel1, K T Vogeley, C Jandeck, F Boegner, P Marx, H C Koch.   

Abstract

Septo-optic dysplasia (or de Morsier syndrome) is a congenital disorder characterised by anomalies in cerebral midline structures, optic nerve hypoplasia, and hormonal deficiencies. Diagnosis should be made early, due to the possibility of treating the hormonal disturbances. We describe here a case with decreased visual acuity, one-sided hemianopia, nystagmus und agenesis of the septum pellucidum and discuss the heterogeneous appearance of this syndrome. There are two theories regarding its pathogenesis. The first postulates simultaneous damage to both cerebral structures and optic nerve development around the 6th week of gestation, while the other favours secondary degeneration of optic nerve fibres due to a cerebral lesion.

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Year:  1998        PMID: 9606688     DOI: 10.1007/s001150050282

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  3 in total

1.  [Visual defects and nystagmus].

Authors:  T Struffert; W Reith
Journal:  Radiologe       Date:  2004-03       Impact factor: 0.635

2.  Distribution of scotoma pattern related to chiasmal lesions with special reference to anterior junction syndrome.

Authors:  Ulrich Schiefer; Melanie Isbert; Eva Mikolaschek; Ingrid Mildenberger; Elke Krapp; Jan Schiller; Solon Thanos; William Hart
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-04-07       Impact factor: 3.117

3.  Diffusion-tensor imaging in septo-optic dysplasia.

Authors:  Felix Schoth; Timo Krings
Journal:  Neuroradiology       Date:  2004-09       Impact factor: 2.804

  3 in total

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