Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/59971
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Cyclin-dependent kinase-like 5 (CDKL5) mutation screening in Rett syndrome and related disorders
Author: White, R.
Ho, G.
Schmidt, S.
Scheffer, I.
Fischer, A.
Yendle, S.
Bienvenu, T.
Nectoux, J.
Ellaway, C.
Darmanian, A.
Tong, X.
Cloosterman, D.
Bennetts, B.
Kalra, V.
Fullston, T.
Gecz, J.
Cox, T.
Christodoulou, J.
Citation: Twin Research and Human Genetics, 2010; 13(2):168-178
Publisher: Australian Academic Press Pty. Ltd.
Issue Date: 2010
ISSN: 1832-4274
1839-2628
Statement of
Responsibility: 
Rose White, Gladys Ho, Swetlana Schmidt, Ingrid E. Scheffer, Alexandra Fischer, Simone C. Yendle, Thierry Bienvenu, Juliette Nectoux, Carolyn J. Ellaway, Artur Darmanian, XingZhang Tong, Desiree Cloosterman, Bruce Bennetts, Veena Kalra, Tod Fullston, Jozef Gecz, Timothy C. Cox and John Christodoulou
Abstract: Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting females almost exclusively and is characterized by a wide spectrum of clinical manifestations. Mutations in the X-linked methyl-CpG-binding protein 2 (MECP2) gene have been found in up to 95% of classical RTT cases and a lesser proportion of atypical cases. Recently, mutations in another X-linked gene, CDKL5 (cyclin-dependent kinase-like 5) have been found to cause atypical RTT, in particular the early onset seizure (Hanefeld variant) and one female with autism. In this study we screened several cohorts of children for CDKL5 mutations, totaling 316 patients, including individuals with a clinical diagnosis of RTT but who were negative for MECP2 mutations (n = 102), males with X-linked mental retardation (n = 9), patients with West syndrome (n = 52), patients with autism (n = 59), patients with epileptic encephalopathy (n = 33), patients with Aicardi syndrome (n = 7) and other patients with intellectual disability with or without seizures (n = 54). In all, seven polymorphic variations and four de novo mutations (c.586C>T [p.S196L]; c.58G>C [p.G20R]; c.2504delC [p.P835fs]; deletion of exons 1 - 3) were identified, and in all instances of the latter the clinical phenotype was that of an epileptic encephalopathy. These results suggest that pathogenic CDKL5 mutations are unlikely to be identified in the absence of severe early-onset seizures and highlight the importance of screening for large intragenic and whole gene deletions.
Keywords: CDKL5; Rett syndrome; infantile spasms; epileptic encephalopathy; intellectual disability; mutation
Rights: Copyright © Australian Academic Press 2010. All Rights Reserved.
RMID: 0020098230
DOI: 10.1375/twin.13.2.168
Appears in Collections:Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.