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GATOR1-related focal cortical dysplasia in epilepsy surgery patients and their families: A possible gradient in severity?

Authors :
Benova, Barbora
Sanders, Maurits W.C.B.
Uhrova-Meszarosova, Anna
Belohlavkova, Anezka
Hermanovska, Barbora
Novak, Vilem
Stanek, David
Vlckova, Marketa
Zamecnik, Josef
Aronica, Eleonora
Braun, Kees P.J.
Koeleman, Bobby P.C.
Jansen, Floor E.
Krsek, Pavel
Source :
European Journal of Paediatric Neurology; Jan2021, Vol. 30, p88-96, 9p
Publication Year :
2021

Abstract

Variants of GATOR1-genes represent a recognised cause of focal cortical dysplasia (FCD), the most common structural aetiology in paediatric drug-resistant focal epilepsy. Reports on familial cases of GATOR1-associated FCD are limited, especially with respect to epilepsy surgery outcomes. We present phenotypical manifestations of four unrelated patients with drug-resistant focal epilepsy, FCD and a first-degree relative with epilepsy. All patients underwent targeted gene panel sequencing as a part of the presurgical work up. Literature search was performed to compare our findings to previously published cases. The children (probands) had a more severe phenotype than their parents, including drug-resistant epilepsy and developmental delay, and they failed to achieve seizure freedom post-surgically. All patients had histopathologically confirmed FCD (types IIa, IIb, Ia). In Patient 1 and her affected father, we detected a known pathogenic NPRL2 variant. In patients 2 and 3 and their affected parents, we found novel likely pathogenic germline DEPDC5 variants. In family 4, we detected a novel variant in NPRL3. We identified 15 additional cases who underwent epilepsy surgery for GATOR1-associated FCD, with a positive family history of epilepsy in the literature; in 8/13 tested, the variant was inherited from an asymptomatic parent. The presented cases displayed a severity gradient in phenotype with children more severely affected than the parents. Although patients with GATOR1-associated FCD are considered good surgical candidates, post-surgical seizure outcome was poor in our familial cases, suggesting that accurate identification of the epileptogenic zone may be more challenging in this subgroup of patients. • We saw severity gradient in phenotype with children more affected than the parents. • Post-surgical seizure outcome was poor in our familial cases. • Accurate identification of the epileptogenic zone is challenging in GATOR1 patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10903798
Volume :
30
Database :
Supplemental Index
Journal :
European Journal of Paediatric Neurology
Publication Type :
Academic Journal
Accession number :
149510723
Full Text :
https://doi.org/10.1016/j.ejpn.2020.12.001