Prenatal diagnosis of mosaic trisomy 13: A case report

被引:0
作者
Eubanks, SR
Kuller, JA
Amjadi, D
Powell, CM
机构
[1] Univ N Carolina, Dept OBGYN, Sch Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Dept Pediat, Chapel Hill, NC 27599 USA
关键词
mosaicism; trisomy; 13; prenatal diagnosis;
D O I
10.1002/(SICI)1097-0223(199809)18:9<971::AID-PD380>3.0.CO;2-P
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
While the clinical features associated with full trisomy 13 have been well characterized, the clinical outcome associated with mosaic trisomy 13 is much less clear. The medical literature reports a broad range of possible clinical outcomes from severe mental retardation and birth defects to normal intelligence. There is no consensus about the typical phenotype in these cases. This makes genetic counselling after prenatal diagnosis of mosaic trisomy 13 particularly difficult. Some of the medical literature attempts to correlate the percentage of trisomic cells in peripheral blood leukocytes or skin fibroblasts with clinical outcome. There have not been case reports correlating the percentage of trisomic amniocytes and clinical outcome. We report the prenatal diagnosis of mosaic trisomy 13 by amniocentesis in which no prenatal ultrasound abnormalities were noted, and autopsy was normal with the exception of the presence of a small ventricular septal defect. (C) 1998 John Wiley & Sons, Ltd.
引用
收藏
页码:971 / 974
页数:4
相关论文
共 50 条
  • [41] Prenatal Clinical Presentation and Genetic Analysis of Partial Trisomy 12: A Case Report
    Mbara, Nnenna
    Fakoya, Adegbenro O.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (08)
  • [42] PRENATAL-DIAGNOSIS AND DYSMORPHIC FINDINGS IN MOSAIC TRISOMY-16
    GARBER, A
    CARLSON, D
    SCHRECK, R
    FISCHELGHODSIAN, N
    HSU, WT
    OEZTAS, S
    PEPKOWITZ, S
    GRAHAM, JM
    PRENATAL DIAGNOSIS, 1994, 14 (04) : 257 - 266
  • [43] PRENATAL-DIAGNOSIS OF TRISOMY-9 MOSAIC PRESENTING AS A CASE OF DANDY-WALKER MALFORMATION
    BUREAU, YA
    FRASER, W
    FOUQUET, B
    PRENATAL DIAGNOSIS, 1993, 13 (02) : 79 - 85
  • [44] Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome
    Chen, Chih-Ping
    Kuo, Yu-Ling
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Shin-Wen
    Wu, Fang-Tzu
    Chen, Li-Feng
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2020, 59 (02): : 327 - 330
  • [45] Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues
    Mazza, Vincenzo
    Latella, Silvia
    Fenu, Valentina
    Ferrari, Paola
    Bonilauri, Carlotta
    Santucci, Sandra
    Percesepe, Antonio
    JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2010, 36 (05) : 1116 - 1120
  • [46] Prenatal diagnosis of trisomy 18: report of 30 cases
    Yang, JH
    Chung, JH
    Shin, JS
    Choi, JS
    Ryu, HM
    Kim, MY
    PRENATAL DIAGNOSIS, 2005, 25 (02) : 119 - 122
  • [47] The natural history of pregnancies with a diagnosis of Trisomy 18 or Trisomy 13; a retrospective case series
    Houlihan, Orla A.
    O'Donoghue, Keelin
    BMC PREGNANCY AND CHILDBIRTH, 2013, 13
  • [48] Increased Fetal Nuchal Translucency as a Sole Clue in the Prenatal Diagnosis of a Fetus with Trisomy 13
    Ki, Kyung-Do
    Kim, So-Ra
    Lee, Woo-In
    FETAL DIAGNOSIS AND THERAPY, 2009, 26 (01) : 54 - 56
  • [49] Reasons for trisomy 13 or 18 births despite the availability of prenatal diagnosis and pregnancy termination
    Gessner, BD
    EARLY HUMAN DEVELOPMENT, 2003, 73 (1-2) : 53 - 60
  • [50] Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome
    Chen, Chih-Ping
    Lin, Chen-Ju
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Yen-Ni
    Chen, Shin-Wen
    Pan, Chen-Wen
    Yang, Chien-Wen
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2017, 56 (02): : 238 - 242