Epilepsy due to autosomal recessive genetic syndromes with widespread or progressive effects (Q86437): Difference between revisions
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Epilepsia devida a uma extensa variedade de condições clínicas que apresentam em comum um defeito genético autossômico recessivo. Majoritariamente representados estão transtornos metabólicos hereditários. Fenótipo varia com a idade do paciente. A semiologia da crise epiléptica e características eletroencefalográficas variam e não são diagnósticos. Exclui síndrome genética expressa primariamente como epilepsia. | |||
| description / en | description / en | ||
Epilepsy due to a wide variety of clinical conditions having in common an autosomal recessive genetic defect. Mostly represented are inherited metabolic disorders. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features vary and are not diagnostic. 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 recessive genetic defect. Mostly represented are inherited metabolic disorders. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features vary and are not diagnostic. Excludes genetic syndromes primarily expressed as epilepsy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1122743842 |
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| English | Epilepsy due to autosomal recessive genetic syndromes with widespread or progressive effects |
Epilepsy due to a wide variety of clinical conditions having in common an autosomal recessive genetic defect. Mostly represented are inherited metabolic disorders. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features vary and are not diagnostic. Excludes genetic syndromes primarily expressed as epilepsy. |
