Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia (Q86435): Difference between revisions
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| description / pt-br | description / pt-br | ||
Epilepsia devida a uma extensa variedade de condições clínicas que apresentam em comum defeito genético ligado ao X. 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 X-linked 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 X-linked 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_1252358703 |
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| English | Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia |
Epilepsy due to a wide variety of clinical conditions having in common an X-linked genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy. |
