Titre :

Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of <i>KCNH5</i>.

Auteur(s) :

Happ, H. C. [Auteur]
Sadleir, L. G. [Auteur]
Zemel, M. [Auteur]
De Valles-Ibáñez, G. [Auteur]
Hildebrand, M. S. [Auteur]
Mcconkie-Rosell, A. [Auteur]
Mcdonald, M. [Auteur]
May, H. [Auteur]
Sands, T. [Auteur]
Aggarwal, V. [Auteur]
Elder, C. [Auteur]
Feyma, T. [Auteur]
Bayat, A. [Auteur]
Møller, R. S. [Auteur]
Fenger, C. D. [Auteur]
Klint Nielsen, J. E. [Auteur]
Datta, A. N. [Auteur]
Gorman, K. M. [Auteur]
King, M. D. [Auteur]
Linhares, N. D. [Auteur]
Burton, B. K. [Auteur]
Paras, A. [Auteur]
Ellard, S. [Auteur]
Rankin, J. [Auteur]
Shukla, A. [Auteur]
Majethia, P. [Auteur]
Olson, R. J. [Auteur]
Muthusamy, K. [Auteur]
Schimmenti, L. A. [Auteur]
Starnes, K. [Auteur]
Sedláčková, L. [Auteur]
Štěrbová, K. [Auteur]
Vlčková, M. [Auteur]
Laššuthová, P. [Auteur]
Jahodová, A. [Auteur]
Porter, B. E. [Auteur]
Couque, N. [Auteur]
Colin, E. [Auteur]
Prouteau, C. [Auteur]
Collet, C. [Auteur]
Smol, Thomas [Auteur]
Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364
Caumes, R. [Auteur]
Vansenne, F. [Auteur]
Bisulli, F. [Auteur]
Licchetta, L. [Auteur]
Person, R. [Auteur]
Torti, E. [Auteur]
Mcwalter, K. [Auteur]
Webster, R. [Auteur]
Gerard, E. E. [Auteur]
Lesca, G. [Auteur]
Szepetowski, P. [Auteur]
Scheffer, I. E. [Auteur]
Mefford, H. C. [Auteur]
Carvill, G. L. [Auteur]

Titre de la revue :

Neurology

Nom court de la revue :

Neurology

Numéro :

100

Pagination :

e603-e615

Date de publication :

2023-09-06

ISSN :

1526-632X

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

Background and Objectives KCNH5 encodes the voltage-gated potassium channel EAG2/Kv10.2. We aimed to delineate the neurodevelopmental and epilepsy phenotypic spectrum associated with de novo KCNH5 variants. Methods We ...
Lire la suite >Background and Objectives KCNH5 encodes the voltage-gated potassium channel EAG2/Kv10.2. We aimed to delineate the neurodevelopmental and epilepsy phenotypic spectrum associated with de novo KCNH5 variants. Methods We screened 893 individuals with developmental and epileptic encephalopathies for KCNH5 variants using targeted or exome sequencing. Additional individuals with KCNH5 variants were identified through an international collaboration. Clinical history, EEG, and imaging data were analyzed; seizure types and epilepsy syndromes were classified. We included 3 previously published individuals including additional phenotypic details. Results We report a cohort of 17 patients, including 9 with a recurrent de novo missense variant p.Arg327His, 4 with a recurrent missense variant p.Arg333His, and 4 additional novel missense variants. All variants were located in or near the functionally critical voltage-sensing or pore domains, absent in the general population, and classified as pathogenic or likely pathogenic using the American College of Medical Genetics and Genomics criteria. All individuals presented with epilepsy with a median seizure onset at 6 months. They had a wide range of seizure types, including focal and generalized seizures. Cognitive outcomes ranged from normal intellect to profound impairment. Individuals with the recurrent p.Arg333His variant had a self-limited drug-responsive focal or generalized epilepsy and normal intellect, whereas the recurrent p.Arg327His variant was associated with infantile-onset DEE. Two individuals with variants in the pore domain were more severely affected, with a neonatal-onset movement disorder, early-infantile DEE, profound disability, and childhood death. Discussion We describe a cohort of 17 individuals with pathogenic or likely pathogenic missense variants in the voltage-sensing and pore domains of Kv10.2, including 14 previously unreported individuals. We present evidence for a putative emerging genotype-phenotype correlation with a spectrum of epilepsy and cognitive outcomes. Overall, we expand the role of EAG proteins in human disease and establish KCNH5 as implicated in a spectrum of neurodevelopmental disorders and epilepsy.Lire moins >

Comité de lecture :

Oui

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

Université de Lille
CHU Lille

Collections :

• Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364

Date de dépôt :

2024-05-15T22:03:19Z
2024-07-01T15:22:41Z