Rubella panencephalitis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Childhood
- Status
- active
A rare chronic encephalitis developing up to several years after congenital rubella virus infection or rubella infection in childhood, characterized by slowly progressive, wide-spread neurological symptoms, like cognitive decline, cerebellar ataxia, spasticity, and seizures, amongst others. Progredient deterioration of the neurological disease eventually leads to the death of the patient.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rubella panencephalitis | |
| fr | Panencéphalite rubéoleuse | |
| de | Röteln-Panenzephalitis | Rubella-Panenzephalitis |
| es | Panencefalitis por rubéola | |
| it | Panencefalite da rosolia | |
| nl | Rubella-panencefalitis | |
| pt | Panencefalite por rubéola | |
| pl | Różyczkowe zapalenie mózgu | |
| cs | Zarděnková panencefalitida | |
| uk | Краснушний паненцефаліт | |
| zh | 风疹性全脑炎 | |
| tr | Kızamıkçık panensefaliti |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B06.0+ | NTBT | attributed | validated |
| ICD-10 | G05.1* | NTBT | attributed | validated |
| ICD-11 | 1F02.0 | NTBT | index | validated |
| MONDO | 19386 | E | validated | |
| UMLS | C0238099 | 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 (3):
- ORPHA:98255Chronic encephalitis
rare neurological diseases - 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 |
|---|---|---|---|---|---|---|
| Cases/families | 20 cases | Worldwide | Case(s) | Validated | 9103895[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | 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/83616
- This record as JSON: /data/d/83616.json