LP185909-1
Fetal triploidy risk
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Description
Triploidy risk refers to the fetus's risk of being affected by triploid syndrome. The risk can be determined by prenatal genetic testing of fetal DNA. Triploid syndrome is caused by the presence of three copies of every chromosome rather than two, for a total of 69 chromosomes rather than the normal 46. The majority of cases are due to two sperm fertilizing a single egg. Most fetuses with triploidy are lost due to miscarriage, and the few infants born with triploidy have multiple birth defects and only survive a few months. [https://www.rarediseases.org] Source: Regenstrief LOINC, NORD: Triploid syndrome
Basic Part Properties
- Part Display Name
- Fetal triploidy risk
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2014-09-12
- Construct for LOINC Short Name
- Trip risk
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | 胎儿三倍体风险 Synonyms: 胎儿三倍体（三倍性、 |
| es-ES | Spanish (Spain) | Riesgo de Triploidía |
| it-IT | Italian (Italy) | Triploidia, rischio Synonyms: Rischio triploidia |
| tr-TR | Turkish (Turkey) | Triploidi riski |
| nl-NL | Dutch (Netherlands) | risico op foetale triploïdie |
LOINC Copyright
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