Epilepsy due to mitochondrial disorders (Q86439): 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 multisystem disorders typically affecting infants, children and young adults, having in common mitochondrial DNA defects. Maternal inheritance with phenotypic variability in families is the general rule. Myoclonic seizures are the common types of seizures. Central nervous system involvement is prominent but with differing clinical manifestations according to the genetic defect. Other clinical conditions (e.g. diabetes, deafness, cardiomyopathy) may be also present. Excludes genetic syndromes primarily expressed as epilepsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1925770864 |
||
| English | Epilepsy due to mitochondrial disorders |
Epilepsy due to multisystem disorders typically affecting infants, children and young adults, having in common mitochondrial DNA defects. Maternal inheritance with phenotypic variability in families is the general rule. Myoclonic seizures are the common types of seizures. Central nervous system involvement is prominent but with differing clinical manifestations according to the genetic defect. Other clinical conditions (e.g. diabetes, deafness, cardiomyopathy) may be also present. Excludes genetic syndromes primarily expressed as epilepsy. |
Statements
CID11:ID_1925770864
0 references
dki-india-ID_1925770864
0 references
Concluído
0 references
13 August 2026
0 references
