Epilepsy due to autosomal dominant genetic syndromes with widespread or progressive effects (Q86434): Difference between revisions
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Epilepsia devido a uma extensa variedade de condições clínicas que, em comum, possuem defeito genético autossômico dominante. Fenótipo varia com a idade do paciente. A semiologia da crise epiléptica e características eletroencefalográficas são indistinguíveis. Exclui síndromes genéticas expressas primariamente como epilepsia. | |||
| description / en | description / en | ||
Epilepsy due to a wide variety of clinical conditions having in common an autosomal dominant genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy. | |||
Revision as of 11:50, 15 August 2026
Epilepsy due to a wide variety of clinical conditions having in common an autosomal dominant genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1970837340 |
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| English | Epilepsy due to autosomal dominant genetic syndromes with widespread or progressive effects |
Epilepsy due to a wide variety of clinical conditions having in common an autosomal dominant genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy. |
