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261. Onchocerciasis associated epilepsy (OAE) in children immigrated to the United States.
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263. Pura Syndrome: A Rare Case of Neonatal Hypotonia with a Novel Multi-Gene Deletion at 5q31.2q31.3 Diagnosed with rWES.
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267. Hyperekplexia secondary to novel SLC6A5 homozygous deletion masquerading as neonatal seizures.
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309. Myalgic encephalomyelitis presenting as orthostatic intolerance in an adolescent.