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    <!-- http://purl.obolibrary.org/obo/DOID_0050709 -->

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        <rdfs:label>early infantile epileptic encephalopathy</rdfs:label>
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        <ns2:IAO_0000115>A neonatal period electroclinical syndrome that is characterized by tonic spasms and partial seizures.</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:9255</oboInOwl:hasDbXref>
        <oboInOwl:creation_date>2012-05-10T10:02:58Z</oboInOwl:creation_date>
        <oboInOwl:hasExactSynonym>Ohtahara syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>OMIM:PS308350</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ORDO:1934</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Early Infantile Epileptic Encephalopathy with Burst-Suppression</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasAlternativeId>DOID:2481</oboInOwl:hasAlternativeId>
        <oboInOwl:hasDefinition>Ohtahara syndrome (also known as early infantile epileptic encephalopathy, EIEE) is a syndrome characterized by frequent intractable seizures and severe early encephalopathy resulting in limited development and reduced life expectancy. Tonic seizures predominate, myoclonic seizures are uncommon, distinguishing this syndrome from early myoclonic encephalopathy. Treatable metabolic etiologies (especially pyridoxine and pyridoxal-5-phosphate disorders) should be excluded early.</oboInOwl:hasDefinition>
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