Back to Search
Start Over
GATOR1-related focal cortical dysplasia in epilepsy surgery patients and their families: A possible gradient in severity?
- 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