Lennox-gastaut Syndrome
What's New
Last Posted: Oct 16, 2024
- Comparative Analysis of Lennox-Gastaut Syndrome With Different Subtypes of Tonic Seizures: A Single-Center Retrospective Cohort Study.
Shiyu Wang, et al. Pediatric neurology 2024 0 132-138 - Clinical features and underlying etiology of children with Lennox-Gastaut syndrome.
Zongpu Zhou, et al. Journal of neurology 2024 0 - Predictors of genetic diagnosis in individuals with developmental and epileptic encephalopathies.
Maria Luiza Benevides, et al. Epilepsy & behavior : E&B 2024 0 109762 - Creating rare epilepsy cohorts using keyword search in electronic health records.
Kristen Barbour et al. Epilepsia 2023 - Clinical and genetic study of developmental and epileptic encephalopathy in Argentinean pediatric patients.
Juanes Matías, et al. Medicina 2022 0 (6) 856-865 - Expanding the neurodevelopmental phenotype of PURA syndrome.
Lee Bo Hoon, et al. American journal of medical genetics. Part A 2017 0 (1) 56-67 - The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant.
Chatron Nicolas, et al. Annals of neurology 2018 0 (5) 926-934 - CHD2-related epilepsy: novel mutations and new phenotypes.
Chen Jiaoyang, et al. Developmental medicine and child neurology 2019 0 (5) 647-653 - Rufinamide efficacy and association with phenotype and genotype in children with intractable epilepsy: A retrospective single center study.
Oesch Gabriela, et al. Epilepsy research 2019 0 106211 - In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth.
Cox Allison J, et al. Genetics research 2019 0 e8
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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