Correction to: Congenital pial AVF along the falx cerebri with complete agenesis of the corpus callosum and bilateral parasagittal pachygyria-polymicrogyria secondary to chronic ischemia

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Neurodevelopmental Outcome of Patients With Agenesis of Corpus Callosum

Background: Agenesis of Corpus Callosum (ACC) is a type of brain dysgenesis with various clinical manifestations. Objectives: This study aimed to investigate the clinical and neurodevelopmental outcomes of patients with ACC. Materials & Methods: In this cross-sectional study, the clinical and neurodevelopmental conditions of 62 patients with complete ACC referred to subspecialty clinics of pe...

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Agenesis of the Corpus Callosum

COMPLETE or partial agenesis of the corpus callosum is uncommon especially in adults; the incidence amongst patients in institutions where numerous air encephalograms are performed is 3% (Carpenter and Drukemiller, 1953). Reil (1812) published the first report of a case, describing the necropsy findings in a 30 year old woman of low mentality; further cases discovered at necropsy were subsequen...

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Parasagittal asymmetries of the corpus callosum.

Significant relationships have been reported between midsagittal areas of the corpus callosum and the degree of interhemispheric transfer, functional lateralization and structural brain asymmetries. No study, however, has examined whether parasagittal callosal asymmetries (i.e. those close to the midline of the brain), which may be of specific functional consequence, are present in the human br...

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Agenesis of the corpus callosum.

COMPLETE or partial agenesis of the corpus callosum is uncommon especially in adults; the incidence amongst patients in institutions where numerous air encephalograms are performed is 3% (Carpenter and Drukemiller, 1953). Reil (1812) published the first report of a case, describing the necropsy findings in a 30 year old woman of low mentality; further cases discovered at necropsy were subsequen...

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ژورنال

عنوان ژورنال: Child's Nervous System

سال: 2019

ISSN: 0256-7040,1433-0350

DOI: 10.1007/s00381-019-04052-z