Research & Literature

Clinical Usefulness of Immunohistochemical Staining of p57 kip2 for the Differential Diagnosis of Complete Mole.

Sasaki S, Sasaki Y, Kunimura T, et al.

BioMed research international 2015; (2015()):905648 doi:10.1155/2015/905648.

Digynic triploidy: utility and challenges of noninvasive prenatal testing.

Fleischer J, Shenoy A, Goetzinger K, et al.

Clinical case reports 2015; (3(6)):406-10 doi:10.1002/ccr3.247.

Uncommon Presentation of Triploidy: A Case Report.

Uzun I, Pata Ö, Unlu C, et al.

Journal of clinical and diagnostic research : JCDR 2015; (9(10)):QD01-2 doi:10.7860/JCDR/2015/14037.6553.

Triploidy: Variation of Phenotype.

Toufaily MH, Roberts DJ, Westgate MN, Holmes LB

American journal of clinical pathology 2016; (145(1)):86-95 doi:10.1093/ajcp/aqv012.

False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review.

Van Opstal D, Srebniak MI, Polak J, et al.

PloS one 2016; (11(1)):e0146794 doi:10.1371/journal.pone.0146794.

A Survey of Perinatal Palliative Care Programs in the United States: Structure, Processes, and Outcomes.

Denney-Koelsch E, Black BP, Côté-Arsenault D, et al.

Journal of palliative medicine 2016; (19(10)):1080-1086 doi:10.1089/jpm.2015.0536.

Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy.

Kolarski M, Ahmetovic B, Beres M, et al.

Medical archives (Sarajevo, Bosnia and Herzegovina) 2017; (71(2)):144-147 doi:10.5455/medarh.2017.71.144-147.

Validation of a targeted next generation sequencing-based comprehensive chromosome screening platform for detection of triploidy in human blastocysts.

Marin D, Zimmerman R, Tao X, et al.

Reproductive biomedicine online 2018; (36(4)):388-395 doi:10.1016/j.rbmo.2017.12.015.

[Application of quantitative fluorescencet-PCR in the prenatal diagnosis of chromosomale aneuploidies].

Qin S, Wang X, Chen X, et al.

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018; (35(2)):228-231 doi:10.3760/cma.j.issn.1003-9406.2018.02.018.

Unexpected finding of uniparental disomy mosaicism in term placentas: Is it a common feature in trisomic placentas?

Van Opstal D, Diderich KEM, Joosten M, et al.

Prenatal diagnosis 2018; (38(12)):911-919 doi:10.1002/pd.5354.

Digynic triploidy in a fetus presenting with semilobar holoprosencephaly.

Chuang TY, Chang SY, Chen CP, et al.

Taiwanese journal of obstetrics & gynecology 2018; (57(6)):881-884 doi:10.1016/j.tjog.2018.11.001.

Single-nucleotide polymorphism microarray detects molar pregnancies in 3% of miscarriages.

Maisenbacher MK, Merrion K, Kutteh WH

Fertility and sterility 2019; (112(4)):700-706 doi:10.1016/j.fertnstert.2019.06.015.

[Efficacy of the Paediatrics Palliative Care Team of Murcia according to the experience of the parents].

Plaza Fornieles M, García-Marcos Barbero P, Galera Miñarro AM, et al.

Anales de pediatria 2020; (93(1)):4-15 doi:10.1016/j.anpedi.2019.07.001.

Comparison between vacuum aspiration and forceps plus blunt curettage for the evacuation of complete hydatidiform moles.

Sato A, Usui H, Shozu M

Taiwanese journal of obstetrics & gynecology 2019; (58(5)):650-655 doi:10.1016/j.tjog.2019.07.012.

Loss of p57KIP2 expression confers resistance to contact inhibition in human androgenetic trophoblast stem cells.

Takahashi S, Okae H, Kobayashi N, et al.

Proceedings of the National Academy of Sciences of the United States of America 2019; (116(52)):26606-26613 doi:10.1073/pnas.1916019116.

Gestational Trophoblastic Neoplasia After Human Chorionic Gonadotropin Normalization Following Molar Pregnancy: A Systematic Review and Meta-analysis.

Albright BB, Shorter JM, Mastroyannis SA, et al.

Obstetrics and gynecology 2020; (135(1)):12-23 doi:10.1097/AOG.0000000000003566.

Prenatal sonographic features can accurately determine parental origin in triploid pregnancies.

Lugthart MA, Horenblas J, Kleinrouweler EC, et al.

Prenatal diagnosis 2020; (40(6)):705-714 doi:10.1002/pd.5666.

Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review.

Massalska D, Bijok J, Kucińska-Chahwan A, et al.

Archives of gynecology and obstetrics 2020; (301(5)):1139-1145 doi:10.1007/s00404-020-05515-4.

An Incidental Ultrasonographic Diagnosis of Partial Hydatidiform Mole in a Old Primigravida: A Case Report.

Thapa S, Rana R, Kumari S

JNMA; journal of the Nepal Medical Association 2020; (58(222)):112-114.

Usefulness of methylation-specific multiplex ligation-dependent probe amplification for identification of parental origin of triploidy.

Massalska D, Ozdarska K, Bijok J, et al.

Journal of human genetics 2020; (65(10)):889-894 doi:10.1038/s10038-020-0784-0.

Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm.

Zhang Z, Hu T, Wang J, et al.

BioMed research international 2019; (2019()):6504159 doi:10.1155/2019/6504159.

Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy.

Fatemi N, Salehi N, Pignata L, et al.

Journal of medical genetics 2021; (58(11)):783-788 doi:10.1136/jmedgenet-2020-106909.

Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.

Chen CP, Chern SR, Wang LK, et al.

Taiwanese journal of obstetrics & gynecology 2020; (59(6)):938-940 doi:10.1016/j.tjog.2020.09.023.

Twin pregnancies discordant for digynic triploidy - A case series.

Massalska D, Bijok J, Kucińska-Chahwan A, et al.

Taiwanese journal of obstetrics & gynecology 2021; (60(1)):139-141 doi:10.1016/j.tjog.2020.11.021.

Evaluation of repeat testing of a non-sequencing based NIPT test on a Finnish general-risk population.

Karlsson F, Ahola T, Dahlberg J, et al.

Acta obstetricia et gynecologica Scandinavica 2021; (100(8)):1497-1500 doi:10.1111/aogs.14125.

Recurrent fetal triploidy: is there a genetic cause?

Fontoura Oliveira A, Torrão MM, Nogueira R, Ferreira M

BMJ case reports 2021; (14(3)) doi:10.1136/bcr-2020-239843.

Factors associated with test failure in pregnant women undergoing cell-free DNA-based testing for fetal trisomy.

Chang J, Qi Q, Zhou X, et al.

Journal of medical screening 2021; (28(4)):411-418 doi:10.1177/09691413211009940.

Gestational trophoblastic neoplasia after human chorionic gonadotropin normalization in a retrospective cohort of 7761 patients in France.

Descargues P, Hajri T, Massardier J, et al.

American journal of obstetrics and gynecology 2021; (225(4)):401.e1-401.e9 doi:10.1016/j.ajog.2021.05.006.

Loss of p57 Expression in Conceptions Other Than Complete Hydatidiform Mole: A Case Series With Emphasis on the Etiology, Genetics, and Clinical Significance.

Xing D, Miller K, Beierl K, Ronnett BM

The American journal of surgical pathology 2022; (46(1)):18-32 doi:10.1097/PAS.0000000000001749.

Prenatal diagnosis of syndromic alobar holoprosencephaly associated with digynic triploidy fetus.

Albu CC, Albu DF, Pătraşcu A, et al.

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2020; (61(4)):1309-1316 doi:10.47162/RJME.61.4.32.

Reply: The missing role of diagnosis of confined placental mosaicism in the management of fetal growth restriction.

Eggenhuizen GM, Go A, Galjaard RJ

Human reproduction update 2021; (28(1)):151-152 doi:10.1093/humupd/dmab033.

The Contribution of QF-PCR and Pathology Studies in the Diagnosis of Diandric Triploidy/Partial Mole.

Benítez L, Pauta M, Badenas C, et al.

Diagnostics (Basel, Switzerland) 2021; (11(10)) doi:10.3390/diagnostics11101811.

Extended survival of a premature infant with a postnatal diagnosis of complete triploidy.

Walsh R, Sharma A

BMJ case reports 2022; (15(2)) doi:10.1136/bcr-2021-244551.

Non-invasive prenatal screening for fetal triploidy using single nucleotide polymorphism-based testing: Differential diagnosis and clinical management in cases showing an extra haplotype.

Kantor V, Jelsema R, Xu W, et al.

Prenatal diagnosis 2022; (42(8)):994-999 doi:10.1002/pd.6169.

Triploidy in a Live-Born Extremely Low Birth Weight Twin: Clinical Aspects.

Vakrilova L, Hitrova-Nikolova S, Bradinova I

Journal of pediatric genetics 2022; (11(3)):227-231 doi:10.1055/s-0040-1716828.

Digynic monoandric triploidy in the setting of recurrent pregnancy loss: a case report and literature review.

Raymond C, Han S, Huang G, et al.

Laboratory medicine 2024; (55(1)):103-105 doi:10.1093/labmed/lmad036.

Polyploidy Phenomenon as a Cause of Early Miscarriages in Abortion Materials.

Yildirim ME, Karakus S, Kurtulgan HK, et al.

Balkan journal of medical genetics : BJMG 2023; (26(1)):5-10 doi:10.2478/bjmg-2023-0002.

Prenatal Diagnosis of Triploidy in Fetus with Unexpected Chromosomal Translocation of Maternal Origin.

Jadhav A, Jadhav Y, Bhairi V, et al.

International journal of molecular and cellular medicine 2023; (12(1)):81-85 doi:10.22088/IJMCM.BUMS.12.1.81.

Evaluation of Combined p57KIP2 Immunohistochemistry and Fluorescent in situ Hybridization Analysis for Hydatidiform Moles Compared with Genotyping Diagnosis.

Usui H, Hoshimoto K, Sato A, et al.

International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2024; (43(5)):474-486 doi:10.1097/PGP.0000000000001000.

Gestational Trophoblastic Disease: Complete versus Partial Hydatidiform Moles.

Gonzalez J, Popp M, Ocejo S, et al.

Diseases (Basel, Switzerland) 2024; (12(7)) doi:10.3390/diseases12070159.

Naturally occurring horse model of miscarriage reveals temporal relationship between chromosomal aberration type and point of lethality.

Lawson JM, Salem SE, Miller D, et al.

Proceedings of the National Academy of Sciences of the United States of America 2024; (121(33)):e2405636121 doi:10.1073/pnas.2405636121.

Gestational Trophoblastic Neoplasia Rate and Its Related Factors in Women With a Partial Hydatidiform Mole at Tudu Hospital, Vietnam.

Vo TM, Hoang TT, Tran HM, Nyamakope K

Cureus 2024; (16(8)):e67495 doi:10.7759/cureus.67495.

Factors, pregnancy outcomes, and management associated with non-reportable results in prenatal cell-free DNA testing.

Yin H, Wang J, Wu X, et al.

Archives of gynecology and obstetrics 2025; (312(1)):197-205 doi:10.1007/s00404-025-07977-w.

Evidence adaptation and tailored implementation of family bereavement support in specialised palliative care: A multi-method study.

Kohler M, Thaqi Q, Kuske S, et al.

International journal of nursing studies advances 2025; (8()):100305 doi:10.1016/j.ijnsa.2025.100305.

What functions do palliative care bereavement services deliver? A scoping review.

Jurgens KE, Currow DC, Tieman J

Palliative care and social practice 2025; (19()):26323524251326947 doi:10.1177/26323524251326947.

Discrepancies Between Pathological Distinction and DNA Genotyping in the Diagnosis of Hydatidiform Moles.

Hasegawa Y, Nagata K, Miura S, et al.

Cureus 2025; (17(6)):e85953 doi:10.7759/cureus.85953.

Thyroid Storm Triggered by Partial Hydatidiform Mole: A Rare and Life-Threatening Complication.

Cox H, Wong M, Preszler J, et al.

AJP reports 2025; (15(2)):e94-e97 doi:10.1055/a-2626-9145.

Screening of triploid in miscarriage tissues using medium-coverage whole genome sequencing with a three-algorithm integrated approach.

Zheng J, Zhang Q, Xu L, et al.

Journal of assisted reproduction and genetics 2025; (42(9)):3133-3142 doi:10.1007/s10815-025-03607-1.

Molar Pregnancy: Early Diagnosis, Clinical Management, and the Role of Referral Centers.

Braga A, Coutinho L, Chagas M, et al.

Diagnostics (Basel, Switzerland) 2025; (15(15)) doi:10.3390/diagnostics15151953.

Beyond grief: Quantifying bereavement needs of rural family caregivers.

Vanderboom C, Holland D, Ingram C, et al.

Palliative & supportive care 2025; (23()):e157 doi:10.1017/S1478951525100205.

Molecular genetic study of triploidy and the hydatidiform mole in pregnancy loss: analysis of 10,000 consecutive cases.

Pushkarev VP, Masycheva AS, Glazyrina EA, et al.

Vavilovskii zhurnal genetiki i selektsii 2025; (29(5)):621-628 doi:10.18699/vjgb-25-67.

The value of quantitative fluorescence polymerase chain reaction for the products of conception in the era of copy number variation sequencing.

Yang S, Zhang H, Wang Y, et al.

Frontiers in genetics 2025; (16()):1750362 doi:10.3389/fgene.2025.1750362.