Selective intrauterine growth restriction
Synonyms: Selective fetal growth restriction · sFGR · sIUGR
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal
- Status
- active
A rare disorder related to monochorionic twin pregnancy characterized by unequal placental sharing leading to growth restriction in one twin according to the following criteria: estimated fetal weight (EFW) of one twin below the 3rd percentile as a solitary parameter, or fulfilment of at least two out of four contributory parameters (EFW of one twin below the 10th percentile, abdominal circumference of one twin below the 10th percentile, EFW discordance of ≥ 25%, umbilical artery pulsatility index of the smaller twin above the 95th percentile). Early severe forms are associated with a significant risk of intrauterine demise or neurological adverse outcome for both twins.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Selective intrauterine growth restriction | Selective fetal growth restriction · sFGR · sIUGR |
| fr | Retard de croissance intra-utérin sélectif | sRCIU |
| de | Selektive intrauterine Wachstumsverzögerung | Selektive fetale Wachstumsrestriktion · sFGR · sIUGR |
| es | Restricción selectiva del crecimiento intrauterino | Restricción selectiva del crecimiento fetal · sFGR · sIUGR |
| it | Ritardo selettivo della crescita prenatale | Ritardo selettivo della crescita fetale · sFGR · sIUGR |
| nl | Selectieve intra-uteriene groeirestrictie | Selectieve foetale groeirestrictie · sFGR · sIUGR |
| pt | Restrição seletiva do crescimento intrauterino | Restrição seletiva do crescimento fetal · sRCF · sRCIU |
| pl | Selektywne zahamowanie wzrostu wewnątrzmacicznego | Selektywne ograniczenie wzrostu wewnątrzmacicznego |
| cs | Selektivní nitroděložní růstová restrikce | = en |
| uk | Селективне внутрішньоутробне обмеження росту | Селективне обмеження росту плода · sFGR · sIUGR |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P02.2 | NTBT | attributed | validated |
| ICD-11 | KA20.1Y | NTBT | attributed | validated |
| MONDO | 0850015 | E | validated | |
| UMLS | C5681824 | 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:617313Rare disorder due to inadequate sharing of the placenta
rare gynecological and obstetric 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 | Validated | 28532678[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/617301
- This record as JSON: /data/d/617301.json