Services on Demand
Journal
Article
Indicators
- Cited by SciELO
- Access statistics
Related links
- Cited by Google
- Similars in SciELO
- Similars in Google
Share
CES Medicina
Print version ISSN 0120-8705
Abstract
ALJURE REALES, Vicente de Jesús et al. Agenesis of the corpus callosum: A little-known topic. CES Med. [online]. 2017, vol.31, n.2, pp.172-179. ISSN 0120-8705. https://doi.org/10.21615/cesmedicina.31.2.6.
Corpus callosum is present only in placental mammals and is composed by approximately 200 - 800 million axons that connect left and right hemispheres. Dysgenesis of corpus callosum may be complete, known as agenesis of the corpus callosum, or partial, known as hypoplasia of the Corpus. Agenesis of the corpus callosum is a malformation that may occur in an isolated way or in association with other disorders of central nervous system. It is one of the most frequent malformations in cerebrum with an estimated prevalence of 1/ 4000 000 births. Among the most frequent clinical findings in patients with agenesis of the Corpus Callosum are mental retardation, visual impairment and seizures. Prenatal diagnosis may be performed through ultrasound and magnetic resonance from week 20 of pregnancy. Postnatal diagnosis may be carried out by performing ultrasound, computerized tomography or magnetic resonance. Currently, there is no specific treatment for ACC. An early stimulation program has been proposed and, if possible, a psychomotor rehabilitation program that offers improvement of motor and learning disorders. Surgical choice is contemplated only for management of associated malformations susceptible of being corrected; symptomatic treatment must be carried out when there are convulsive syndromes.
Keywords : Agenesis of Corpus Callosum; Congenital abnormalities; Nervous system malformation; Prenatal diagnosis.