Natural History of Fetal Trisomy 13 After Prenatal Diagnosis

被引:12
作者
Barry, Sinead C. [1 ]
Walsh, Colin A. [2 ]
Burke, Annette L. [1 ]
McParland, Peter [2 ]
McAuliffe, Fionnuala M. [3 ]
Morrison, John J. [1 ]
机构
[1] Natl Univ Ireland Galway, Galway Univ Hosp, Dept Obstet & Gynaecol, Galway, Ireland
[2] Natl Matern Hosp, Fetal Med Unit, Dublin 2, Ireland
[3] UCD Obstet & Gynaecol, Sch Med, Dublin, Ireland
关键词
fetal trisomy 13; fetal medicine; neonatal outcome; PATAU SYNDROME; SURVIVAL;
D O I
10.1002/ajmg.a.36824
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There are currently limited data describing the natural history and outcome for fetal trisomy 13 diagnosed prenatally. The aim of this study was to evaluate the fetal and neonatal outcome for pregnancies with an established prenatal diagnosis of fetal trisomy 13, and a parental decision for continuation of the pregnancy. To this end, the obstetric and neonatal outcome data for such pregnancies, diagnosed at two referral Fetal Medicine Centers, were retrospectively obtained and examined. During the study period, there were 45 cases of trisomy 13 diagnosed at both units, of which 26 (56%) continued with the pregnancy to its natural outcome. There were 12 intrauterine deaths in the cohort resulting in a rate of 46.2% of intrauterine lethality. Conversely, the live birth rate was 53.8%. For infants born alive, neonatal death on day 1 of life occurred in 78.6% of cases. The overall early neonatal mortality rate was 93%. There was one infant death at 6 weeks of age and no survival noted beyond this period. These data provide reliable information for parental counseling pertaining to risk of intrauterine death when trisomy 13 is diagnosed prenatally. These data also indicate that the survival outcome is worse than that previously accepted from studies of postnatal follow up of live born infants with this diagnosis. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:147 / 150
页数:4
相关论文
共 9 条
[1]   Natural history of fetal trisomy 18 after prenatal diagnosis [J].
Burke, Annette L. ;
Field, Katie ;
Morrison, John J. .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2013, 98 (02) :F152-F154
[2]   Changes in fetal prevalence and outcome for trisomies 13 and 18: a population-based study over 23 years [J].
Irving, Claire ;
Richmond, Sam ;
Wren, Christoper ;
Longster, Caitlin ;
Embleton, Nicholas D. .
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2011, 24 (01) :137-141
[3]   Natural Outcome of Trisomy 13, Trisomy 18, and Triploidy After Prenatal Diagnosis [J].
Lakovschek, Ioana Claudia ;
Streubel, Berthold ;
Ulm, Barbara .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (11) :2626-2633
[4]   TRISOMY 13 (D1) SYNDROME - STUDIES ON PARENTAL AGE SEX RATIO AND SURVIVAL [J].
MAGENIS, RE ;
HECHT, F ;
MILHAM, S .
JOURNAL OF PEDIATRICS, 1968, 73 (02) :222-+
[5]   Ultrasound detection and perinatal outcome of fetal trisomies 21, 18 and 13 in the absence of a routine fetal anomaly scan or biochemical screening [J].
Moran, CJ ;
Tay, JB ;
Morrison, JJ .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2002, 20 (05) :482-485
[6]   Clinical Features and Prognosis of a Sample of Patients With Trisomy 13 (Patau Syndrome) From Brazil [J].
Petry, Patricia ;
Polli, Janaina B. ;
Mattos, Vinicius F. ;
Rosa, Rosana C. M. ;
Zen, Paulo R. G. ;
Graziadio, Carla ;
Paskulin, Giorgio A. ;
Rosa, Rafael F. M. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (06) :1278-1283
[7]   Survival of Texas Infants Born With Trisomies 21, 18, and 13 [J].
Vendola, Catherine ;
Canfield, Mark ;
Daiger, Stephen P. ;
Gambello, Michael ;
Hashmi, S. Shahrukh ;
King, Terri ;
Noblin, Sarah J. ;
Waller, D. Kim ;
Hecht, Jacqueline T. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (02) :360-366
[8]   Survival of Trisomy 18 (Edwards Syndrome) and Trisomy 13 (Patau Syndrome) in England and Wales: 2004-2011 [J].
Wu, Jianhua ;
Springett, Anna ;
Morris, Joan K. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161 (10) :2512-2518
[9]   NATURAL-HISTORY OF TRISOMY-13 [J].
WYLLIE, JP ;
WRIGHT, MJ ;
BURN, J ;
HUNTER, S .
ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 71 (04) :343-345