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Eur J Med Genet. 2012 May;55(5):299-306. doi: 10.1016/j.ejmg.2012.04.002. Epub 2012 Apr 22.

Molecular bases and clinical spectrum of early infantile epileptic encephalopathies.

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1
Department of Pediatrics, Cedars Sinai Medical Center, 8700 Beverly Blvd, Los Angeles, CA 90048, USA. jane.tavyev@cshs.org

Abstract

Epilepsy can be a challenging diagnosis to make in the neonatal and infantile periods. Seizures in this age group may be due to a serious underlying cause that results in an epileptic encephalopathy. Early infantile epileptic encephalopathy (EIEE) is a progressive neurologic condition that exhibits concomitant cognitive and motor impairment, and is often associated with severe intellectual disability. This condition belongs to the group of age-dependent epileptic encephalopathies, and thus the clinical and electro-encephalographic features change with age as the central nervous system evolves. The molecular bases and the clinical spectrum associated with the early infantile epileptic encephalopathies continue to expand as new genetic discoveries are made. This review will highlight the molecular etiologies of early infantile epileptic encephalopathy, and the clinical and electro-encephalographic changes that take place in these epileptic phenotypes as the brain develops.

PMID:
22548976
DOI:
10.1016/j.ejmg.2012.04.002
[Indexed for MEDLINE]
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