Title of article
SEPTO-OPTICDYSPLASIA WITH AN ANTERIOR ENCEPHALOCELE AND INTACT SEPTUM PELLUCIDUM: A CASE REPORT
Author/Authors
Razavi، Z. نويسنده Associate Professor, Pediatric Endocrinologist, Hamedan University of Medical Sciences ,
Issue Information
فصلنامه با شماره پیاپی - سال 2008
Pages
4
From page
57
To page
60
Abstract
Objective
The diagnosis of de Morsier syndrome or septo-optic dysplasia is made on the
basis of the diagnosis of optic nerve hypoplasia. Septo-optic dysplasia is defined
by a variable combination of dysgenesis of midline brain structures including
optic nerve hypoplasia and hypothalamic-pituitary dysfunction often associated
with a wide variety of brain malformations of cortical development.
The importance of direct ophthalmoscopy of optic nerve abnormalities is
stressed, as well as of magnetic resonance imaging, which has become a
guideline in the classification of this syndrome
This article reports a 19-year-old female with bilateral optic nerve hypoplasia,
anterior encephalocele and intact septum pellucidum. She was diagnosed with
diabetes insipidus, short stature and the history of seizure.
Journal title
Iranian Journal of Child Neurology (IJCN)
Serial Year
2008
Journal title
Iranian Journal of Child Neurology (IJCN)
Record number
673640
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