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ORIGINAL ARTICLE

The phenotypic spectrum of YWHAG-related epilepsy: From mild febrile seizures to severe developmental delay and epileptic encephalopathy

Quanzhen Tan

Quanzhen Tan

Children's Medical Centre, Peking University First Hospital, Beijing, China

Quanzhen Tan and Miaomiao Cheng contributed equally to this work.

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Miaomiao Cheng

Miaomiao Cheng

Children's Medical Centre, Peking University First Hospital, Beijing, China

Quanzhen Tan and Miaomiao Cheng contributed equally to this work.

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Ying Yang

Ying Yang

Children's Medical Centre, Peking University First Hospital, Beijing, China

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Ting Wang

Ting Wang

Children's Medical Centre, Peking University First Hospital, Beijing, China

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Shijia Ouyang

Shijia Ouyang

Children's Medical Centre, Peking University First Hospital, Beijing, China

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Changhao Liu

Changhao Liu

Children's Medical Centre, Peking University First Hospital, Beijing, China

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Xiaoling Yang

Xiaoling Yang

Children's Medical Centre, Peking University First Hospital, Beijing, China

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Wenwei Liu

Wenwei Liu

Children's Medical Centre, Peking University First Hospital, Beijing, China

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Ye Wu

Ye Wu

Children's Medical Centre, Peking University First Hospital, Beijing, China

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Yuehua Zhang

Corresponding Author

Yuehua Zhang

Children's Medical Centre, Peking University First Hospital, Beijing, China

Correspondence

Yuehua Zhang, Children's Medical Centre, Peking University First Hospital, Beijing 102627, China.

Email: [email protected]

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First published: 05 April 2025

Abstract

Aim

To explore the phenotypic spectrum and refine the genotype–phenotype correlation of YWHAG-related epilepsy.

Method

This study used a retrospective cohort design to evaluate the clinical data of 15 patients with epilepsy and YWHAG variants in our Chinese cohort (nine males, six females; median age: 6 years 4 months; range: 1 year 6 months–12 years 8 months) and 40 patients with epilepsy with YWHAG variants from published studies (21 males, 19 females; median age: 10 years; range: 3 years–67 years).

Results

In our cohort, seven variants were de novo and five were new. Seizure onset for 14 of 15 patients occurred within the first 2 years of life. Nine of 15 patients had a history of febrile seizures. Seizure types included generalized tonic–clonic seizures (GTCS) and myoclonic seizures. Developmental delay was present in 11 of 15 patients. Three patients were diagnosed with febrile seizures plus, one was diagnosed with myoclonic epilepsy in infancy, one had infantile epileptic spasm syndrome, and 10 had developmental and epileptic encephalopathy that could not be further classified into a specific epilepsy syndrome. Seizures were controlled in 7 of 15 patients; most were treated with valproate and levetiracetam. Collectively, in our cohort and from published studies, most variants (38 of 55, 69.1%) were located in the highly conserved triad (HCT) domain of Arg132-Arg57-Tyr133. Mild phenotypes were more frequently observed in patients with variants located outside the HCT domain, with a significant difference of 70.6% versus 27.0% (p < 0.01).

Interpretation

Most patients with YWHAG variants were diagnosed during infancy. The most common seizure types were GTCS and myoclonic seizures. The phenotypic spectrum of epilepsy ranged from mild febrile seizures to severe developmental delay and epileptic encephalopathy. Most variants were localized in the HCT domain; variants residing outside the HCT domain were correlated with milder phenotypes.

Graphical Abstract

DATA AVAILABILITY STATEMENT

The data that supports the findings of this study are available in the supplementary material of this article.

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