Epilepsy with myoclonic-astatic seizures (Q41211): Difference between revisions
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Revision as of 07:17, 13 August 2026
Epilepsy beginning between the second and fifth year of life in a previously normal child with family history of seizures, that initially manifests as tonic-clonic seizures with myoclonic-astatic seizures beginning several weeks later. These seizures are characterised by a sudden loss of muscular tonus associated with forward or backward propulsion that may result in injury to the face and head if the patient falls.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.22 |
||
| English | Epilepsy with myoclonic-astatic seizures |
Epilepsy beginning between the second and fifth year of life in a previously normal child with family history of seizures, that initially manifests as tonic-clonic seizures with myoclonic-astatic seizures beginning several weeks later. These seizures are characterised by a sudden loss of muscular tonus associated with forward or backward propulsion that may result in injury to the face and head if the patient falls. |
