Please use this identifier to cite or link to this item:
|Title:||Chromosomal abnormalities and epilepsy: a review for clinicians and gene hunters.||Austin Authors:||Singh, Rita;Gardner, R J McKinlay;Crossland, Kathryn M;Scheffer, Ingrid E ;Berkovic, Samuel F||Affiliation:||Department of Medicine (Neurology), The University of Melbourne, Austin and Repatriation Medical Centre, Australia||Issue Date:||1-Feb-2002||Publication information:||Epilepsia; 43(2): 127-40||Abstract:||We analyzed databases on chromosomal anomalies and epilepsy to identify chromosomal regions where abnormalities are associated with clinically recognizable epilepsy syndromes. The expectation was that these regions could then be offered as targets in the search for epilepsy genes.The cytogenetic program of the Oxford Medical Database, and the PubMed database were used to identify chromosomal aberrations associated with seizures and/or EEG abnormalities. The literature on selected small anomalies thus identified was reviewed from a clinical and electroencephalographic viewpoint, to classify the seizures and syndromes according to the current International League Against Epilepsy (ILAE) classification.There were 400 different chromosomal imbalances described with seizures or EEG abnormalities. Eight chromosomal disorders had a high association with epilepsy. These comprised: the Wolf-Hirschhorn (4p-) syndrome, Miller-Dieker syndrome (del 17p13.3), Angelman syndrome (del 15q11-q13), the inversion duplication 15 syndrome, terminal deletions of chromosome 1q and 1p, and ring chromosomes 14 and 20. Many other segments had a weaker association with seizures. The poor quality of description of the epileptology in many reports thwarted an attempt to make precise karyotype-phenotype correlations.We identified certain chromosomal regions where aberrations had an evident association with seizures, and these regions may be useful targets for gene hunters. New correlations with specific epilepsy syndromes were not revealed. Clinicians should continue to search for small chromosomal abnormalities associated with specific epilepsy syndromes that could provide important clues for finding epilepsy genes, and the epileptology should be rigorously characterized.||Gov't Doc #:||11903458||URI:||http://ahro.austin.org.au/austinjspui/handle/1/9391||Journal:||Epilepsia||URL:||https://pubmed.ncbi.nlm.nih.gov/11903458||Type:||Journal Article||Subjects:||Chromosome Aberrations
Databases as Topic
|Appears in Collections:||Journal articles|
Show full item record
checked on Feb 7, 2023
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.