Fetal parvovirus syndrome
Synonyms: Mother-to-child transmission of parvovirus syndrome · Parvovirus antenatal infection
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal, Neonatal
- Status
- active
Foetal parvovirus syndrome is a foetopathy likely to occur when a pregnant woman is infected by parvovirus B19. In adults, the virus causes a butterfly erythema infectiosum (also called Fifth Disease; 'slapped cheek disease') and flu-like symptoms with symmetric polyarthralgias, which usually do not warrant prenatal diagnosis.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fetal parvovirus syndrome | Mother-to-child transmission of parvovirus syndrome · Parvovirus antenatal infection |
| fr | Embryopathie à parvovirus | Infection anténatale au parvovirus |
| de | Parvovirus-Embryopathie | Parvovirus-Infektion durch Mutter-Kind-Übertragung · Parvovirus-Infektion, vorgeburtliche |
| es | Síndrome de parvovirus fetal | Infección prenatal por parvovirus · Transmisión materna del síndrome de parvovirus |
| it | Embriopatia da parvovirus | Infezione prenatale da parvovirus |
| nl | Foetaal parvovirussyndroom | Antenatale parvovirusinfectie · Transmissie van moeder op kind van parvovirussyndroom |
| pt | Síndrome de parvovírus fetal | Infeção pré-natal por parvovírus |
| pl | Parwowirusowy zespół płodu | Parwowirusowa infekcja płodowa |
| cs | Fetální parvovirový syndrom | Prenatální parvovirová infekce |
| uk | Фетальний парвовірусний синдром | Передача парвовірусного синдрому від матері до дитини · Парвовірусна антенатальна інфекція |
| zh | 胎儿巨细小病毒综合征 | 母婴传播型细小病毒综合征 |
| tr | Fetal parvovirus sendromu | Parvovirus antenatal enfeksiyon · Parvovirüs sendromunun anneden çocuğa geçişi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P35.8 | NTBT | attributed | validated |
| ICD-11 | KA62.7 | E | specific | validated |
| MONDO | 0017453 | E | validated | |
| MeSH | C536301 | E | validated | |
| UMLS | C2931167 | E | validated | |
| GARD | 4236 | 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:232035Infectious embryofetopathy
rare developmental anomalies during embryogenesis; rare infectious diseases; rare teratologic disorders - ORPHA:138059Teratogenic Pierre Robin syndrome
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases; rare surgical maxillo-facial 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 | 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
9 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0001903 | Anemia | |
| HP:0001541 | Ascites | |
| HP:0001789 | Hydrops fetalis | |
| HP:0001873 | Thrombocytopenia | |
| Occasional (29-5%) | ||
| HP:0000478 | Abnormality of the eye | |
| HP:0000504 | Abnormality of vision | |
| HP:0001639 | Hypertrophic cardiomyopathy | |
| HP:0010880 | Increased nuchal translucency | |
| HP:0001511 | Intrauterine growth retardation | |
Run the differential on the 4 obligate / very frequent terms
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/295
- This record as JSON: /data/d/295.json