Miscarriage chromosome testing: Indications, benefits and methodologies

Seminars in Perinatology - Tập 43 - Trang 101-104 - 2019
Dana B. McQueen1, Ruth B. Lathi1,2
1Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, Northwestern University, Chicago, IL, United States
2Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, Stanford University, Palo Alto, United States

Tài liệu tham khảo

Benkhalifa, 2005, Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro, Prenatal Diagnosis, 25, 894, 10.1002/pd.1230 Roman, 1984, Fetal loss rates and their relation to pregnancy order, J Epidemiol Commun Health, 38, 29, 10.1136/jech.38.1.29 Stirrat, 1990, Recurrent miscarriage, Lancet, 336, 673, 10.1016/0140-6736(90)92159-F Stephenson, 1996, Frequency of factors associated with habitual abortion in 197 couples, Fertil Steril, 66, 24, 10.1016/S0015-0282(16)58382-4 Sugiura-Ogasawara, 2012, Abnormal embryonickaryotype is the most frequent cause of recurrent miscarriage, Hum Reprod, 27, 2297, 10.1093/humrep/des179 Popescu, 2018, Recurrent pregnancy loss evaluation combined with 24-chromosome microarray of miscarriage tissue provides a probable or definite cause of pregnancy loss in over 90% of patients, Human Reprod, 33, 579, 10.1093/humrep/dey021 Stephenson, 2002, Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case-control study, Hum Reprod, 17, 446, 10.1093/humrep/17.2.446 Levy, 2014, Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis, Obstet Gynecol, 124, 202, 10.1097/AOG.0000000000000325 Jacobs, 1997, Turner syndrome: a cytogenetic and molecular study, Ann Hum Genet, 61, 471, 10.1017/S0003480097006507 Bernardi, 2012, Is chromosome testing of the second miscarriage cost saving? A decision analysis of selective versus universal recurrent pregnancy loss evaluation, Fertil Steril, 98, 156, 10.1016/j.fertnstert.2012.03.038 Foyouzi, 2012, Cost-effectiveness of cytogenetic evaluation of products of conception in the patient with a second pregnancy loss, Fertil Steril, 98, 151, 10.1016/j.fertnstert.2012.04.007 Bell, 1999, Cyogenetic diagnosis of normal 46, XX karyotypes in spontaneous abortions frequently may be misleading, Fert STeril, 71, 334, 10.1016/S0015-0282(98)00445-2 Lathi, 2012, Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytogenetics, PloS One, 7, e31282, 10.1371/journal.pone.0031282 Benkhalifa, 2005, Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro, Prenatal Diagn, 25, 894, 10.1002/pd.1230 Dhillon, 2014, Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta-analysis, BJOG, 121, 11, 10.1111/1471-0528.12382 Shah, 2017, Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens, Fertil Steril, 107, 1028, 10.1016/j.fertnstert.2017.01.022 Murugappan, 2014, Separation of miscarriage tissue from maternal decidua for chromosome analysis, Fertil Steril, 102, e9, 10.1016/j.fertnstert.2014.07.006 McNally, 2016, Patient experience with karyotyping after first trimester miscarriage: a national survey, Reprod Med, 61, 128