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• W1982982007 abstract "Mutations of the cyclin-dependent kinase-like 5 gene (CDKL5), reported almost exclusively in female subjects, have been recently found to be the cause of a phenotype overlapping Rett syndrome with early-onset epileptic encephalopathy. We describe the first CDKL5 mutation detected in a male individual with 47,XXY karyotype. This previously unreported, de novo, mutation truncates the large CDKL5 COOH-terminal region, thought to be crucial for the proper sub-cellular localization of the CDKL5 protein. The resulting phenotype is characterized by a severe early-onset epileptic encephalopathy, global developmental delay, and profound intellectual and motor impairment with features reminiscent of Rett syndrome. In light of the data presented we discuss the possible phenotypic modulatory effects of the supernumerary wild type X allele and pattern of X chromosome inactivation and stress the importance of considering the causal involvement of CDKL5 in developmentally delayed males with early-onset seizures. © 2009 Wiley-Liss, Inc." @default.
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• W1982982007 date "2009-02-01" @default.
• W1982982007 modified "2023-10-16" @default.
• W1982982007 title "A novel<i>CDKL5</i>mutation in a 47,XXY boy with the early-onset seizure variant of Rett syndrome" @default.
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• W1982982007 doi "https://doi.org/10.1002/ajmg.a.32606" @default.
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