Electroencephalography in congenital malformations of the central nervous system

Author:

Campos Patrícia1,Cruz Guillermo2,Lizarraga Rodolfo3,Bancalari Ernesto4,Guillen Daniel4,Castañeda Carlos5

Affiliation:

1. Universidad Peruana Cayetano Heredia

2. Instituto Peruano de Seguridad Social

3. Hospital de la Sanidad de las Fuerzas Policiales

4. Hospital Cayetano Heredia

5. Instituto Nacional de Enfermedades Neurológicas

Abstract

We studied clinical and EEG features of 36 cases with congenital malformations of the CNS. Patients were followed at the outpatient clinic of Hospital Cayetano Heredia and of Hogar Clinica San Juan de Dios in Lima-Peru, from January 1984 to June 1992. Eighty percent of the patients had convulsive syndromes and mental retardation. The most frequent malformation was agenesis of corpus callosum, and it was not possible to find a "typical" EEG pattern. The second were porencephalic cysts, with a good clinical-EEG correlation. There were two typical cases of schizencephaly, one of hemimegalencephaly with good prognosis, and one of holoprosencephaly. The results are compared to those obtained for a series we previously reported. Data discussed take into account reports on the subject registered in the literature. It is concluded that EEG is an useful method to evaluate possible CNS malformations in developing countries.

Publisher

FapUNIFESP (SciELO)

Subject

Neurology,Neurology (clinical)

Reference32 articles.

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3. Electroencephalographic abnormalities in non tumor hydrocephalus;Bogacz J;EEG Clin Neurophysiol,1962

4. The influence of associated cerebral lesions on the morphology of the acallosal brain: a pathological and encephalographic study;Brun A;Neuroradiology,1973

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Holoprosencephaly: A Review;American Journal of Electroneurodiagnostic Technology;2002-06

2. Schizencephaly: clinical and imaging features in 30 infantile cases;Brain and Development;2000-12

3. Agenesis of Corpus Callosum: Clinical Description and Etiology;Journal of Child Neurology;2000-06

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