Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/17379
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Type: Journal article
Title: Early onset seizures and Rett-like features associated with mutations in CDKL5
Author: Evans, J.
Archer, H.
Colley, J.
Ravn, K.
Nielsen, J.
Kerr, A.
Williams, E.
Christodoulou, J.
Gecz, J.
Jardine, P.
Wright, M.
Pilz, D.
Lazarou, L.
Cooper, D.
Sampson, J.
Butler, R.
Whatley, S.
Clarke, A.
Citation: European Journal of Human Genetics, 2005; 13(10):1113-1120
Publisher: Nature Publishing Group
Issue Date: 2005
ISSN: 1018-4813
1476-5438
Statement of
Responsibility: 
Julie C Evan, Hayley L Archer, James P Colley, Kirstine Ravn, Jytte Bieber Nielsen, Alison Kerr, Elizabeth Williams, John Christodoulou, Jozef Gécz, Philip E Jardine, Michael J Wright, Daniela T Pilz, Lazarus Lazarou,David N Cooper, Julian R Sampson, Rachel Butler, Sharon D Whatley and Angus J Clarke
Abstract: Mutations in the CDKL5 gene (also known as STK9) have recently been shown to cause early onset epilepsy and severe mental retardation (ISSX or West syndrome). Patients with CDKL5 mutations sometimes also show features similar to those seen in Rett Syndrome (RTT). We have screened the CDKL5 gene in 94 patients with RTT or a RTT-like phenotype who had tested negative for MECP2 mutations (13 classical RTT female subjects, 25 atypical RTT female subjects, 40 RTT-like female and 16 RTT-like male subjects; 33 of the patients had early onset seizures). Novel pathogenic CDKL5 mutations were identified in three girls, two of whom had initially been diagnosed with the early onset seizure variant of RTT and the other with early onset seizures and some features of RTT. In addition, the 33 patients with early seizures were screened for the most common mutations in the ARX gene but none were found. Combining our three new cases with the previously published cases, 13/14 patients with CDKL5 mutations presented with seizures before the age of 3 months.
Keywords: Humans; Epilepsy; Rett Syndrome; Protein-Serine-Threonine Kinases; Homeodomain Proteins; Transcription Factors; RNA Splice Sites; DNA Mutational Analysis; Mutation; Child; Child, Preschool; Infant; Infant, Newborn; Female; Male
RMID: 0020051052
DOI: 10.1038/sj.ejhg.5201451
Appears in Collections:Paediatrics publications

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