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

Journal of Neuroradiology

Volumn 23, Issue 2, 1996, Pages 79-81

  Sener, R Nuri ^a  

^a EGE UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

Author keywords

brain; callosal agenesis; MR studies; septo optic dysplasia

Indexed keywords

ARTICLE; CASE REPORT; CORPUS CALLOSUM AGENESIS; HOLOPROSENCEPHALY; HUMAN; INFANT; KALLMANN SYNDROME; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; SCHIZENCEPHALY; SEPTOOPTIC DYSPLASIA;

BRAIN; CORPUS CALLOSUM; FACIES; HOLOPROSENCEPHALY; HUMANS; INFANT; MALE; OPTIC CHIASM; OPTIC DISK; OPTIC NERVE DISEASES; SEIZURES; SEPTUM PELLUCIDUM; SYNDROME;

EID: 10344260799     PISSN: 01509861     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

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3. Sener RN. Septo-optic dysplasia associated with total absence of the corpus callosum : MR and CT features Eur Radiol 1993 ; 3 : 551-3.
4. Lahat E, Strauss S, Tadmor R, Bistritzer T Infantil spasms in patient with septo-optic dysplasia, partial agenesis of the corpus callosum and an interhemispheric cyst. Clin Neurol Neurosurg 1992 ; 94 : 165-7.
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7. Barkovich AJ. Apparent atypical callosal dysgenesis : analysis of MR findings in six cases and their relationship to holoprosencephaly. AJNR 1990 , 11 : 333-9.