Literature DB >> 8948159

Septo-optic dysplasia (de Morsier's syndrome) associated with total callosal absence. A new type of the anomaly.

R N Sener1.   

Abstract

It is currently believed that there are two subsets of septo-optic dysplasia (de Morsier's syndrome), one with schizencephaly and the other without schizencephaly. Also, some authors consider septo-optic dysplasia as a mild form of holo-prosencephaly. This article describes a third form of the anomaly which is associated with total callosal absence. Two patients similar to this one have previously been reported. None of these three patients had interhemispheric fusion in any form, excluding holoprosencephaly. They had normal facies. All of them presented with seizures, and no hormonal abnormality was found. This new clinicoradiological type of the anomaly is suggested to be labelled as calloso-septo-optic or calloso-optic dysplasia.

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Year:  1996        PMID: 8948159

Source DB:  PubMed          Journal:  J Neuroradiol        ISSN: 0150-9861            Impact factor:   3.447


  1 in total

1.  Six adult patients with septo-optic dysplasia and drug-resistant epilepsy: Clinical findings and course.

Authors:  Mashael AlKhateeb; Richard McLachlan; Jorge Burneo; David Diosy; Seyed Mirsattari
Journal:  Epilepsy Behav Case Rep       Date:  2017-04-19
  1 in total

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