Eating reflex epilepsy
Synonyms: Eating epilepsy · Eating seizures
- Type
- Disease
- Group
- Disorder
- Age of onset
- All ages
- Status
- active
A rare reflex epilepsy characterized by in most cases complex partial seizures triggered by different components of eating, such as the sight of food, proprioceptive, olfactory or gustatory sensations, chewing, salivation, and gastric distension after food intake. The seizures may be idiopathic or associated with symptomatic localization-related epilepsies.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Eating reflex epilepsy | Eating epilepsy · Eating seizures |
| fr | Epilepsie de l'alimentation | |
| de | Ess-Reflexepilepsie | Ess-Epilepsie · Ess-Krampfanfälle |
| es | Epilepsia refleja de la alimentación | Crisis por la ingesta de alimentos · Epilepsia por la ingesta de alimentos |
| it | Epilessia riflessa da assunzione di cibo | |
| nl | Voedingsgeïnduceerde reflexepilepsie | Voedingsgeïnduceerde epilepsie · Voedingsgeïnduceerde epileptische aanvallen |
| pt | Convulsões alimentares | |
| pl | Napady padaczkowe wyzwalane jedzeniem | = en |
| cs | Záchvaty vyvolané jídlem | = en |
| uk | Епілепсія з рефлекторними судомами, повязаними зі споживанням їжі | Харчова епілепсія · Харчові напади |
| zh | 进食反射性癫痫 | 进餐性惊厥 |
| tr | Yemek yeme epilepsisi | Yemek yeme epilepsisi · Yeme nöbetleri |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G40.5 | NTBT | attributed | validated |
| ICD-11 | 8A61.40 | NTBT | index | validated |
| MONDO | 0015645 | E | validated | |
| UMLS | C0393725 | 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:310Reflex epilepsy
rare genetic diseases; rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 1 000 000 | 0.5 / 100 000 | Worldwide | Value and class | Validated | Source: 33080481[PMID]_27986877[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/166418
- This record as JSON: /data/d/166418.json