Recurrent mutations in the CDKL5 gene: Genotype-phenotype relationships.

Détails

ID Serval
serval:BIB_45D3E965D7B2
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Recurrent mutations in the CDKL5 gene: Genotype-phenotype relationships.
Périodique
American Journal of Medical Genetics. Part A
Auteur(s)
Bahi-Buisson N., Villeneuve N., Caietta E., Jacquette A., Maurey H., Matthijs G., Van Esch H., Delahaye A., Moncla A., Milh M., Zufferey F., Diebold B., Bienvenu T.
ISSN
1552-4833 (Electronic)
ISSN-L
1552-4825
Statut éditorial
Publié
Date de publication
2012
Volume
158A
Numéro
7
Pages
1612-1619
Langue
anglais
Notes
Publication types: Journal ArticlePublication Status: ppublish
Résumé
Mutations in the cyclin-dependent kinase-like 5 gene (CDKL5) have been described in epileptic encephalopathies in females with infantile spasms with features that overlap with Rett syndrome. With more than 80 reported patients, the phenotype of CDKL5-related encephalopathy is well-defined. The main features consist of seizures starting before 6 months of age, severe intellectual disability with absent speech and hand stereotypies and deceleration of head growth, which resembles Rett syndrome. However, some clinical discrepancies suggested the influence of genetics and/or environmental factors. No genotype-phenotype correlation has been defined and thus there is a need to examine individual mutations. In this study, we analyzed eight recurrent CDKL5 mutations to test whether the clinical phenotype of patients with the same mutation is similar and whether patients with specific CDKL5 mutations have a milder phenotype than those with other CDKL5 mutations. Patients bearing missense mutations in the ATP binding site such as the p.Ala40Val mutation typically walked unaided, had normocephaly, better hand use ability, and less frequent refractory epilepsy when compared to girls with other CDKL5 mutations. In contrast, patients with mutations in the kinase domain (such as p.Arg59X, p.Arg134X, p.Arg178Trp/Pro/Gln, or c.145 + 2T > C) and frameshift mutations in the C-terminal region (such as c.2635_2636delCT) had a more severe phenotype with infantile spasms, refractory epileptic encephalopathy, absolute microcephaly, and inability to walk. It is important for clinicians to have this information when such patients are diagnosed. © 2012 Wiley Periodicals, Inc.
Pubmed
Web of science
Création de la notice
22/07/2012 21:49
Dernière modification de la notice
03/03/2018 16:46
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