Congenital Epstein-Barr virus infection
Synonyms: Antenatal EBV infection · Antenatal Epstein-Barr virus infection · Congenital EBV infection · Mother-to-child transmission of Epstein-Barr virus infection
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- Status
- active
A rare infectious disease that causes no clinical manifestations in the majority of infants. Indeed, the occurrence of congenital infection with EBV has never been demonstrated conclusively and must be very rare. One case has been reported to present after birth, multiple congenital anomalies (micrognathia, cryptorchidism, central cataracts), dystrophy, generalized hypotonia, hepatosplenomegaly, diffuse petechiae and hematomas and multiple areas of metaphysitis of the long bones at birth. A low birth weight was also reported. No specific follow-up of the fetus is recommended following maternal EBV primary-infection.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital Epstein-Barr virus infection | Antenatal EBV infection · Antenatal Epstein-Barr virus infection · Congenital EBV infection · Mother-to-child transmission of Epstein-Barr virus infection |
| fr | Infection congénitale au virus d'Epstein-Barr | Infection anténatale au virus d'Epstein-Barr · Infection congénital à EBV · Infection anténatale au EBV |
| de | Epstein-Barr Virusinfektion, kongenitale | EBV-Infektion, kongenitale · EBV-Infektion, vorgeburtliche · Epstein-Barr Virusinfektion durch Mutter-Kind-Übertragung · Epstein-Barr Virusinfektion, pränatale |
| es | Infección congénita por el virus de Epstein-Barr | Infección congénita por EBV · Infección prenatal por EBV · Infección prenatal por el virus de Epstein-Barr · Transmisión materna de la infección por el virus Epstein-Barr |
| it | Infezione congenita da virus di Epstein-Barr | Infezione prenatale da virus di Epstein-Barr |
| nl | Congenitale infectie met Epstein-Barrvirus | Antenatale EBV-infectie · Antenatale infectie met Epstein-Barrvirus · Congenitale EBV-infectie · Overdracht van moeder op kind van infectie met Epstein-Barrvirus |
| pt | Infeção congénita por vírus Epstein-Barr | Infeção pré-natal por vírus Epstein-Barr |
| pl | Wrodzone zakażenie wirusem Epsteina-Barra | Prenatalne zakażenie wirusem Epsteina-Barra |
| cs | Vrozená infekce virem Epsteina-Barrové | Antenatální Epsteina-Barrové virová infekce · Vrozená infekce virem Epstein-Barrové · Antenatální Epstein-Barrové virová infekce |
| uk | Вроджена інфекція вірусу Епштейна-Барр | Антенатальна інфекція EBV · Антенатальна інфекція вірусу Епштейна-Барр · Вроджена ВЕБ-інфекція · Передача вірусної інфекції Епштейна-Барр від матері до дитини |
| zh | 先天性EB病毒感染 | 母婴传播型Epstein-Barr病毒感染 |
| tr | Doğumsal Epstein-Barr virüsü enfeksiyonu | Antenatal EBV enfeksiyonu · Doğumsal EBV enfeksiyonu · Antenatal Epstein-Barr virüsü enfeksiyonu · Epstein-Barr virüs enfeksiyonunun anneden çocuğa bulaşması |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P35.8 | NTBT | attributed | validated |
| ICD-11 | KA62.1 | E | specific | validated |
| MONDO | 0019094 | E | validated | |
| UMLS | C4274357 | 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:163585Rare viral disease
rare infectious 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
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/70596
- This record as JSON: /data/d/70596.json