Literature DB >> 1612653

EEG recognition of holoprosencephaly and Aicardi syndrome.

K N Shah1, S Rajadhyaksha, V S Shah, M Wakde.   

Abstract

Two cases of alobar holoprosencephaly and two of Aicardi syndrome are reported for their highly specific electroencephalographic (EEG) changes. The asynchronous sharp waves and spikes over the frontal regions with decreasing gradient of potential to the occipital leads were seen in alobar holoprosencephaly while burst suppression pattern with total asynchrony between the two hemispheres was seen in Aicardi syndrome. Even though EEG changes cannot be pathognomic of any abnormality, it is suggested that as in conditions like subacute sclerosing panencephalitis and petitmal epilepsy, so also in alobar holoprosencephaly and Aicardi syndrome, the characteristic features seen on EEG may provide the initial clue to the correct diagnosis.

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Year:  1992        PMID: 1612653     DOI: 10.1007/bf02760909

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  4 in total

1.  EEG IN HOLOPROSENCEPHALY (ARHINENCEPHALY).

Authors:  W DEMYER; P T WHITE
Journal:  Arch Neurol       Date:  1964-11

2.  EEG recognition of Aicardi's syndrome.

Authors:  R G Fariello; R W Chun; J M Doro; J R Buncic; J S Prichard
Journal:  Arch Neurol       Date:  1977-09

3.  The Aicardi syndrome.

Authors:  J Dennis; B D Bower
Journal:  Dev Med Child Neurol       Date:  1972-06       Impact factor: 5.449

4.  Heterogeneity of clinical severity and molecular lesions in Aicardi syndrome.

Authors:  J A Neidich; R L Nussbaum; R J Packer; B S Emanuel; J M Puck
Journal:  J Pediatr       Date:  1990-06       Impact factor: 4.406

  4 in total
  1 in total

1.  Paradoxical downward seizure pattern on amplitude-integrated electroencephalogram.

Authors:  M Ito; H Kidokoro; Y Sugiyama; Y Sato; J Natsume; K Watanabe; M Hayakawa
Journal:  J Perinatol       Date:  2014-08       Impact factor: 2.521

  1 in total

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