Congenital Oculomotor Apraxia, first described by Cogan in 1953, is a quite rare disorder characterized by iperfixation and absence of horizontal eye movements, with conservation of vertical movements. Ethiopathogenetic and clinical aspects of this disorder are still unclear. We describe ophthalmological, neurodevelopmental and neuro-radiological characteristics of two cases at our observation at 7 and 10 months respectively, which explain polimorfism and complexity of this disorders.
Congenital Oculomotor Apraxia (cogan-syndrome) - Report of 2 Cases
BIANCHI, PAOLO EMILIO;
1995-01-01
Abstract
Congenital Oculomotor Apraxia, first described by Cogan in 1953, is a quite rare disorder characterized by iperfixation and absence of horizontal eye movements, with conservation of vertical movements. Ethiopathogenetic and clinical aspects of this disorder are still unclear. We describe ophthalmological, neurodevelopmental and neuro-radiological characteristics of two cases at our observation at 7 and 10 months respectively, which explain polimorfism and complexity of this disorders.File in questo prodotto:
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