Etiological Analysis and Classification of 108 patients with Infantile Epileptic Spasms Syndrome based on the 2017 International League Against Epilepsy Classification
The basic difficulty encountered during the ILAE classification of this large group of patients was to classify the genetic causes that result in structural anomalies and congenital metabolic diseases. Previous experience, along with the findings of the present study, suggest that ILAE 2017 etiologic classification may be revised, genetic reasons resulting in structural and/or metabolic abnormalities should be classified under the name of genetic origin and that genetic titles should be divided into subgroups such as genetic metabolic, genetic structural, and other genetic categories.
Authors
- Emek Uyur Yalçın (ORCID: https://orcid.org/0000-0001-6071-6375)
- Nilüfer Eldeş
- Yüksel Yılmaz (ORCID: https://orcid.org/0000-0002-0548-9322)
- Olcay I. Unver (ORCID: https://orcid.org/0000-0003-3472-9759)
- Derya Güder
- Kutlay Gür
Institutions
- Mardin Artuklu University (TR)
- Zeynep Kamil Hospital (TR)
- İskenderun Technical University (TR)
- Marmara University (TR)
Publication Details
- Journal
- Nöro Psikiyatri Arşivi
- Published
- 2025-01-01
- DOI
- https://doi.org/10.29399/npa.28983
- Primary Topic
- Attention Deficit Hyperactivity Disorder
- Type
- article
- Field-Weighted Citation Impact
- 0.00