Trisomy 9 associated with maternal serum screening results positive for trisomy 18. Case report and review of the literature

被引:4
|
作者
Priola, Valentina [1 ]
De Vivo, Antonio [1 ]
Imbesi, Giovanna [1 ]
Azzerboni, Andrea [1 ]
Triolo, Onofrio [1 ]
机构
[1] Univ Messina, Dept Gynecol Obstet Sci & Reprod Med, Messina, Italy
关键词
nonmosaic trisomy 9; maternal serum screening; prenatal diagnosis;
D O I
10.1002/pd.1847
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:1167 / 1169
页数:3
相关论文
共 30 条
  • [21] Is intermediate risk really intermediate? Comparison of karyotype and non-invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening
    Bulbul, Gul Alkan
    Kirtis, Emine
    Kandemir, Hulya
    Sanhal, Cem Yasar
    Uzuner, Sezin Yakut
    Karauzum, Sibel Berker
    Mendilcioglu, Ibrahim Inanc
    JOURNAL OF GENETIC COUNSELING, 2025, 34 (02)
  • [22] Ultrasound diagnosis of central nervous system anomalies (bifid choroid plexus, ventriculomegaly, Dandy-Walker malformation) associated with multicystic dysplastic kidney disease in a trisomy 9 fetus: Case report with literature review
    Tonni, Gabriele
    Grisolia, Giampaolo
    JOURNAL OF CLINICAL ULTRASOUND, 2013, 41 (07) : 441 - 447
  • [23] Partial trisomy of the long arm of chromosome 1: Prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature
    Cambosu, Francesca
    Capobianco, Giampiero
    Fogu, Giuseppina
    Bandiera, Pasquale
    Pirino, Alessio
    Moro, Maria Antonietta
    Sanna, Raimonda
    Soro, Giovanna
    Dessole, Margherita
    Montella, Andrea
    JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2013, 39 (02) : 592 - 597
  • [24] PRENATAL DIAGNOSIS OF A DE NOVO PARTIAL TRISOMY 6q AND PARTIAL MONOSOMY 18p ASSOCIATED WITH CEPHALOCELE: A CASE REPORT
    Karaman, A.
    Karaman, B.
    Cetinkaya, A.
    Karaman, S.
    Demirci, O.
    BALKAN JOURNAL OF MEDICAL GENETICS, 2020, 23 (01) : 99 - 102
  • [25] Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
    Chen, Chih-Ping
    Chen, Yi-Yung
    Chern, Schu-Rern
    Wu, Peih-Shan
    Su, Jun-Wei
    Chen, Yu-Ting
    Lee, Chen-Chi
    Chen, Li-Feng
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2013, 52 (03): : 395 - 400
  • [26] A FETAL CYSTIC NECK MASS ASSOCIATED WITH MATERNAL TUBEROUS SCLEROSIS - CASE-REPORT AND LITERATURE-REVIEW
    VANOPPEN, ACC
    BRESLAUSIDERIUS, EJ
    STOUTENBEEK, P
    TERGUNNE, AJP
    MERKUS, JMWM
    PRENATAL DIAGNOSIS, 1991, 11 (12) : 915 - 920
  • [27] Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome
    Chen, Chih-Ping
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Shin-Wen
    Wu, Fang-Tzu
    Chen, Li-Feng
    Chen, Yun-Yi
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2022, 61 (01): : 141 - 145
  • [28] Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with positive NIPT and CVS results for trisomy 2, maternal uniparental disomy 2, perinatal progressive decrease of the aneuploid cell line, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, intrauterine growth restriction and a favorable fetal outcome
    Chen, Chih-Ping
    Wu, Fang-Tzu
    Chern, Schu-Rern
    Wu, Peih-Shan
    Lee, Chen-Chi
    Pan, Chen-Wen
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2023, 62 (04): : 571 - 576
  • [29] Prenatal diagnosis of 9q34.3 microdeletion-associated Kleefstra syndrome in a pregnancy complicated by polyhydramnios: A case report and literature review
    Tai, Yi-Yun
    Chen, Chih-Ling
    Wu, Chen-Tu
    Lee, Chien-Nan
    Lin, Shin-Yu
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (06): : 948 - 952
  • [30] Report Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result
    Chen, Chih-Ping
    Ko, Tsang-Ming
    Wang, Liang-Kai
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Shin-Wen
    Wu, Fang-Tzu
    Chen, Li-Feng
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2021, 60 (04): : 775 - 777