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Article

Chromosomal microarray in unexplained severe early onset epilepsy - A single centre cohort.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society - 1 Jul 2015

Allen Nicholas M, Conroy Judith, Shahwan Amre, Ennis Sean, Lynch Bryan, Lynch Sally A, King Mary D

Abstract excerpt

BACKGROUND: Severe early onset epilepsy may lead to impaired cognitive and motor development, and consists of a group of specific and overlapping electro-clinical phenotypes which may be the result of an inborn error of metabolism, congenital or acquired structural brain lesion, known chromosomal or mono-genetic disorder. A significant proportion of cases however remain unexplained, representing a major...

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PMID: 25920948
DOI: 10.1016/j.ejpn.2015.03.010

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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