Parental decisions following the prenatal diagnosis of sex chromosome abnormalities

被引:41
作者
Hamamy, HA [1 ]
Dahoun, S [1 ]
机构
[1] CMU, Div Genet Med, Lab Cytogenet, CH-1211 Geneva 4, Switzerland
来源
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY | 2004年 / 116卷 / 01期
关键词
sex chromosome abnormalities; parental decisions; prenatal diagnosis; pregnancy termination; cytogenctics;
D O I
10.1016/j.ejogrb.2003.12.029
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To report parental decisions regarding pregnancy termination following the prenatal diagnosis of a sex chromosome abnormality (SCA) in the fetus. Methods: Retrospective collection of data from records of 61 families receiving genetic counseling after prenatal diagnosis of a sex chromosome abnormality in the fetus in the Division of Medical Genetics, University Hospital of Geneva during the time period 1980-2001. Results: Among 61 couples with a prenatal diagnosis of a sex chromosome abnormality (SCA), 44 couples (72.1%) decided to terminate pregnancy. Pregnancy termination rates were 100, 73.9, 70, 50 and 42.9% for Turner syndrome, Klinefelter syndrome, 47,XXX females, 47,XYY males, and mosaic cases, respectively. In all 11 cases with a fetal abnormality seen on ultrasound, pregnancy was terminated. Termination rates were higher among couples with a higher mean number of previous children. Maternal age and year of test did not influence parental decisions. Conclusions: Parental decision to terminate a pregnancy for a fetus with a SCA varied by type of sex chromosome abnormality, by presence of fetal ultrasound anomalies, and by the mean number of previous children. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:58 / 62
页数:5
相关论文
共 24 条
[1]   What parents are told after prenatal diagnosis of a sex chromosome abnormality: interview and questionnaire study [J].
Abramsky, L ;
Hall, S ;
Levitan, J ;
Marteau, TM .
BRITISH MEDICAL JOURNAL, 2001, 322 (7284) :463-466
[2]   THE CENTRALIZED PRENATAL GENETICS SCREENING-PROGRAM OF NEW-YORK-CITY .3. THE 1ST 7,000 CASES [J].
BENN, PA ;
HSU, LYF ;
CARLSON, A ;
TANNENBAUM, HL .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 20 (02) :369-384
[3]  
Christian SM, 2000, PRENATAL DIAG, V20, P37
[4]  
Drake H, 1996, CLIN GENET, V49, P134
[5]   DETERMINANTS OF PARENTAL DECISIONS TO ABORT FOR CHROMOSOME-ABNORMALITIES [J].
DRUGAN, A ;
GREB, A ;
JOHNSON, MP ;
KRIVCHENIA, EL ;
UHLMANN, WR ;
MOGHISSI, KS ;
EVANS, MI .
PRENATAL DIAGNOSIS, 1990, 10 (08) :483-490
[6]   Pregnancy outcome and prenatal diagnosis of sex chromosome abnormalities in Hawaii, 1986-1999 [J].
Forrester, MB ;
Merz, RD .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 119A (03) :305-310
[7]   Prenatal and postnatal prevalence of Turner's syndrome: A registry study [J].
Gravholt, CH ;
Juul, S ;
Naeraa, RW ;
Hansen, J .
BMJ-BRITISH MEDICAL JOURNAL, 1996, 312 (7022) :16-21
[8]  
Hall S., 2001, Community Genet, V4, P233, DOI 10.1159/000064198
[9]   PARENTAL DECISIONS REGARDING TERMINATION OF PREGNANCY FOLLOWING PRENATAL DETECTION OF SEX-CHROMOSOME ABNORMALITY [J].
HOLMESSIEDLE, M ;
RYYNANEN, M ;
LINDENBAUM, RH .
PRENATAL DIAGNOSIS, 1987, 7 (04) :239-244
[10]   Parental decisions of prenatally detected sex chromosome abnormality [J].
Kim, YJ ;
Park, SY ;
Han, JY ;
Kim, MY ;
Yang, JH ;
Choi, KH ;
Kim, YM ;
Kim, JM ;
Ryu, HM .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2002, 17 (01) :53-57