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Genetic epilepsy with febrile seizures plus: refining the spectrum

Version 2 2024-06-06, 12:07
Version 1 2018-05-30, 10:33
journal contribution
posted on 2024-06-06, 12:07 authored by Y-H Zhang, R Burgess, JP Malone, GC Glubb, KL Helbig, L Vadlamudi, S Kivity, Z Afawi, A Bleasel, P Grattan-Smith, BE Grinton, ST Bellows, DF Vears, JA Damiano, H Goldberg-Stern, AD Korczyn, LM Dibbens, EK Ruzzo, MS Hildebrand, SF Berkovic, IE Scheffer
OBJECTIVE: Following our original description of generalized epilepsy with febrile seizures plus (GEFS+) in 1997, we analyze the phenotypic spectrum in 409 affected individuals in 60 families (31 new families) and expand the GEFS+ spectrum. METHODS: We performed detailed electroclinical phenotyping on all available affected family members. Genetic analysis of known GEFS+ genes was carried out where possible. We compared our phenotypic and genetic data to those published in the literature over the last 19 years. RESULTS: We identified new phenotypes within the GEFS+ spectrum: focal seizures without preceding febrile seizures (16/409 [4%]), classic genetic generalized epilepsies (22/409 [5%]), and afebrile generalized tonic-clonic seizures (9/409 [2%]). Febrile seizures remains the most frequent phenotype in GEFS+ (178/409 [44%]), followed by febrile seizures plus (111/409 [27%]). One third (50/163 [31%]) of GEFS+ families tested have a pathogenic variant in a known GEFS+ gene. CONCLUSION: As 37/409 (9%) affected individuals have focal epilepsies, we suggest that GEFS+ be renamed genetic epilepsy with febrile seizures plus rather than generalized epilepsy with febrile seizures plus. The phenotypic overlap between GEFS+ and the classic generalized epilepsies is considerably greater than first thought. The clinical and molecular data suggest that the 2 major groups of generalized epilepsies share genetic determinants.

History

Journal

Neurology

Volume

89

Pagination

1210-1219

Location

Philadelphia, Pa.

ISSN

0028-3878

eISSN

1526-632X

Language

eng

Publication classification

C Journal article, C1.1 Refereed article in a scholarly journal

Copyright notice

2017, American Academy of Neurology

Issue

12

Publisher

Lippincott Williams & Wilkins