Digynic monoandric triploidy in the setting of recurrent pregnancy loss: a case report and literature review.
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DOI: 10.1093/labmed/lmad036
Abstract: Triploidy is a genetic occurrence in which the chromosome count is 3n = 69 with a double (2n) chromosomal contribution to the conceptus from one parent. Such pregnancies are usually nonviable and are estimated to account for… read more here.
Keywords: triploidy; setting recurrent; monoandric triploidy; recurrent pregnancy ... See more keywords
Triploid pregnancy–Clinical implications
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DOI: 10.1111/cge.14003
Abstract: Triploidy is a life‐limiting genetic aberration resulting from an extra haploid set of chromosomes of paternal (diandric triploidy) or maternal origin (digynic triploidy). Triploidy affects around 1%–2% of all conceptions. The majority of cases is… read more here.
Keywords: origin; clinical implications; triploid pregnancy; triploidy ... See more keywords
Extended survival of a premature infant with a postnatal diagnosis of complete triploidy
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DOI: 10.1136/bcr-2021-244551
Abstract: Triploidy is a common chromosomal abnormality that usually results in spontaneous abortion. Liveborn infants usually die within hours or days of birth. We present the case of a female infant born at 30 weeks and… read more here.
Keywords: complete triploidy; triploidy; diagnosis complete; infant ... See more keywords