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- W4366709747 abstract "Congenital disorders of glycosylation (CDG) are a group of rare inherited metabolic disorders caused by defects in various defects of protein or lipid glycosylation pathways. The symptoms and signs of CDG usually develop in infancy. Epilepsy is commonly observed in CDG individuals and is often a presenting symptom. These epilepsies can present across the lifespan, share features of refractoriness to antiseizure medications, and are often associated with comorbid developmental delay, psychomotor regression, intellectual disability, and behavioral problems. In this review, we discuss CDG and infantile epilepsy, focusing on an overview of clinical manifestations and electroencephalographic features. Finally, we propose a tiered approach that will permit a clinician to systematically investigate and identify CDG earlier, and furthermore, to provide genetic counseling for the family." @default.
- W4366709747 created "2023-04-24" @default.
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- W4366709747 date "2023-05-01" @default.
- W4366709747 modified "2023-10-16" @default.
- W4366709747 title "Congenital disorders of glycosylation and infantile epilepsy" @default.
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- W4366709747 doi "https://doi.org/10.1016/j.yebeh.2023.109214" @default.
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