Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia (Q86435): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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 |
||
| 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. |
Statements
CID11:ID_1252358703
0 references
dki-india-ID_1252358703
0 references
Concluído
0 references
13 August 2026
0 references
