Fetal cardiac anomalies and genetic syndromes

被引:30
作者
Pajkrt, E
Weisz, B
Firth, HV
Chitty, LS
机构
[1] UCL Hosp, Inst Child Hlth, London, England
[2] Addenbrookes Hosp, Dept Med Genet, Cambridge, England
关键词
fetal ultrasound; cardiac abnormalities; genetic syndromes;
D O I
10.1002/pd.1067
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cardiac anomalies may occur in isolation or can be part of a genetic syndrome. In this article, we describe some of the genetic syndromes commonly associated with cardiac anomalies where there are other sonographic features that may aid accurate prenatal diagnosis. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:1104 / 1115
页数:12
相关论文
共 144 条
[1]   TUBEROUS SCLEROSIS IN WESTERN SWEDEN - A POPULATION STUDY OF CASES WITH EARLY-CHILDHOOD ONSET [J].
AHLSEN, G ;
GILLBERG, IC ;
LINDBLOM, R ;
GILLBERG, C .
ARCHIVES OF NEUROLOGY, 1994, 51 (01) :76-81
[2]  
Aitken DA, 1999, PRENATAL DIAG, V19, P706, DOI 10.1002/(SICI)1097-0223(199908)19:8<706::AID-PD613>3.0.CO
[3]  
2-W
[4]   NOONAN SYNDROME [J].
ALLANSON, JE .
JOURNAL OF MEDICAL GENETICS, 1987, 24 (01) :9-13
[5]   Low first-trimester pregnancy-associated plasma protein-A and Cornelia de Lange syndrome [J].
Arbuzova, S ;
Nikolenko, M ;
Krantz, D ;
Hallahan, T ;
Macri, J .
PRENATAL DIAGNOSIS, 2003, 23 (10) :864-864
[6]   THE CLINICAL AND GENETIC SPECTRUM OF THE HOLT-ORAM SYNDROME (HEART-HAND SYNDROME) [J].
BASSON, CT ;
COWLEY, GS ;
SOLOMON, SD ;
WEISSMAN, B ;
POZNANSKI, AK ;
TRAILL, TA ;
SEIDMAN, JG ;
SEIDMAN, CE .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (13) :885-891
[7]   Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome [J].
Basson, CT ;
Bachinsky, DR ;
Lin, RC ;
Levi, T ;
Elkins, JA ;
Soults, J ;
Grayzel, D ;
Kroumpouzou, E ;
Traill, TA ;
LeblancStraceski, J ;
Renault, B ;
Kucherlapati, R ;
Seidman, JG ;
Seidman, CE .
NATURE GENETICS, 1997, 15 (01) :30-35
[8]   Prenatal diagnosis of cardiosplenic syndromes: a 10-year experience [J].
Berg, C ;
Geipel, A ;
Smrcek, J ;
Krapp, M ;
Germer, U ;
Kohl, T ;
Gembruch, U ;
Baschat, AA .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2003, 22 (05) :451-459
[9]   Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC) [J].
Bergmann, C ;
Zerres, K ;
Peschgens, T ;
Senderek, J ;
Hörnchen, H ;
Rudnik-Schöneborn, S .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 121A (02) :151-155
[10]   A population-based study of the 22q11.2 deletion: Phenotype, incidence, and contribution to major birth defects in the population [J].
Botto, LD ;
May, K ;
Fernhoff, PM ;
Correa, A ;
Coleman, K ;
Rasmussen, SA ;
Merritt, RK ;
O'Leary, LA ;
Wong, LY ;
Elixson, EM ;
Mahle, WT ;
Campbell, RM .
PEDIATRICS, 2003, 112 (01) :101-107