Benign occipital epilepsy of childhood - early onset variant (disorder) | | Benign occipital epilepsy of childhood - early onset variant | | Panayiotopoulos syndrome Early-onset benign childhood occipital epilepsy Benign childhood occipital epilepsy Panayiotopoulos type
| | A rare genetic neurological disorder characterized by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalized convulsion. Autonomic status epilepticus may be the only clinical event in some cases. | | benigne occipitale epilepsie Panayiotopoulos-type | | benigne nachtelijke occipitale epilepsie op kinderleeftijd Panayiotopoulos-syndroom benign nocturnal childhood occipital epilepsy syndrome syndroom van Panayiotopoulos
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| Id | 230387008 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | G40.0 | Rule | TRUE | Advice | ALWAYS G40.0 | Correlation | SNOMED CT source code to target map code correlation not specified |
Target | Q07.8 | Rule | TRUE | Advice | ALWAYS Q07.8 | Correlation | SNOMED CT source code to target map code correlation not specified |
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