Benign focal seizures of adolescence
Synonyms: Adolescent benign focal crisis · BFSA
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare epilepsy typically characterized by isolated focal motor and somatosensory seizures. Less frequently other focal seizure types, with or without secondary generalization, have been described. The seizures usually happen when the patient is awake and take a benign course. The condition is transitory, interictal examinations are normal, and there is usually no family history of epilepsy.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Benign focal seizures of adolescence | Adolescent benign focal crisis · BFSA |
| fr | Epilepsie partielle bénigne de l'adolescent | Crises partielles bénignes de l'adolescent · Epilepsie focale bénigne de l'adolescent |
| de | Benigne fokale Adoleszenten-Epilepsie | BFSA · BFAA · BFAE · Benigne fokale Anfälle in der Adoleszenz |
| es | Epilepsia focal benigna de la adolescencia | Crisis focales benignas del adolescente |
| it | Convulsioni focali benigne dell'adolescenza | Crisi focale benigna dell'adolescente · BFSA |
| nl | Goedaardige focale insulten in adolescentie | Adolescente goedaardige focale crisis · Benigne focale epilepsie in adolescentie · BFSA |
| pt | Convulsões focais benignas do adolescente | |
| pl | Łagodne ogniskowe drgawki młodzieńcze | Młodzieńczy łagodny kryzys ogniskowy |
| cs | Benigní fokální záchvaty v dospívání | Adolescentní benigní fokální krize |
| uk | Доброякісні фокальні судоми в підлітковому віці | Підлітковий доброякісний вогнищевий криз |
| zh | 良性局灶性青少年癫痫 | 青少年良性局灶性癫痫 |
| tr | Selim fokal ergenlik nöbetleri | Ergen selim odak krizi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G40.8 | NTBT | attributed | validated |
| ICD-11 | 8A6Y | NTBT | index | validated |
| MONDO | 0015471 | E | validated | |
| UMLS | C4275141 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98259Childhood-onset epilepsy syndrome
rare genetic diseases; rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1544
- This record as JSON: /data/d/1544.json