La Crosse encephalitis
Synonyms: Californian encephalitis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
An acute arboviral infection caused by the <i>La Crosse bunyavirus</i> transmitted by an infected mosquito, usually observed in infants, children or adolescents (6 months to 16 years), and characterized by the onset of flulike symptoms such as fever, chills, nausea, vomiting, headache, and abdominal pain, followed by the onset of encephalitis characterized by somnolence, obtundation, and even seizures, focal neurologic signs (asymmetrical reflexes or Babinski signs), paralysis or even coma. CE can leave sequelae such as residual epilepsy and neurocognitive deficits.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | La Crosse encephalitis | Californian encephalitis |
| fr | Encéphalite de La Crosse | Encéphalite de Californie |
| de | Kalifornische Enzephalitis | |
| es | Encefalitis de La Crosse | Encefalitis californiana |
| it | Encefalite di La Crosse | Encefalite californiana |
| nl | La Crosse-encefalitis | Californië-encefalitis |
| pt | Encefalite da Califórnia | |
| pl | Zapalenie mózgu La Crosse | Kalifornijskie zapalenie mózgu |
| cs | La Crossova encefalitida | Kalifornská encefalitida |
| uk | Енцефаліт Ла-Кросса | Каліфорнійський енцефаліт |
| zh | 大地病毒脑炎 | 加利福尼亚脑炎 |
| tr | La Crosse ensefaliti | Kaliforniya ensefaliti |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A83.5 | NTBT | attributed | validated |
| ICD-11 | 1C8D | NTBT | index | validated |
| MONDO | 0019378 | E | validated | |
| MeSH | D004670 | E | validated | |
| UMLS | C0276379 | E | validated | |
| GARD | 10925 | E | validated | |
| MedDRA | 10014584 | 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 (2):
- ORPHA:166490Infectious disease with epilepsy
rare neurological diseases - ORPHA:98252Infectious encephalitis
rare neurological diseases; rare infectious diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 1.91 / 100 000 | Canada | Value and class | Validated | Canada Public Health Agency[OTHER] |
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | 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/83483
- This record as JSON: /data/d/83483.json