PENTALOGY-OF-CANTRELL AND ASSOCIATED MIDLINE ANOMALIES - A POSSIBLE VENTRAL MIDLINE DEVELOPMENTAL FIELD

被引:113
作者
CARMI, R
BOUGHMAN, JA
机构
[1] UNIV MARYLAND, DEPT PEDIAT, BALTIMORE, MD 21201 USA
[2] UNIV MARYLAND, DEPT EPIDEMIOL & PREVENT MED, BALTIMORE, MD 21201 USA
[3] BEN GURION UNIV NEGEV, SOROKA MED CTR, CLIN GENET UNIT, IL-84105 BEER SHEVA, ISRAEL
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 42卷 / 01期
关键词
PENTALOGY-OF-CANTRELL; MIDLINE DEVELOPMENTAL FIELD; CLEFT LIP AND PALATE; NEURAL TUBE DEFECTS; ECTOPIA CORDIS;
D O I
10.1002/ajmg.1320420118
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Five cases of the Pentalogy of Cantrell (PC), ascertained through the Baltimore-Washington population-based study of infants with congenital cardiovascular malformations, represent a regional prevalence of 5.5/1 million liveborn infants for this disorder. Three of these patients had cleft lip with or without palate. Review of the reported literature of the Pentalogy of Cantrell and various combinations of the anomalies within the spectrum of this pentad suggests that the PC defines a specific midline ventral developmental field. Cleft lip with or without cleft palate and encephalocele tend to specifically associate with ventral midline anomalies within the spectrum of PC. These associations might either illustrate the previously observed tendency of specific occurrence of certain combinations of midline defects or represent defined subunits of the midline developmental field.
引用
收藏
页码:90 / 95
页数:6
相关论文
共 41 条
[1]  
BAKER ME, 1984, J ULTRAS MED, V3, P525
[2]   TRISOMY-18 ASSOCIATED WITH ECTOPIA CORDIS AND OCCIPITAL MENINGOCELE [J].
BICK, D ;
MARKOWITZ, RI ;
HORWICH, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (03) :805-810
[3]   Ectopia cordis - Report of a case and review of the literature [J].
Blatt, ML ;
Zeldes, M .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1942, 63 (03) :515-529
[4]  
BRENNAN PL, 1970, OCT AM COLL SURG
[5]  
BRITT A, 1952, BRIT MED J, V1, P1175
[6]  
CANTRELL JR, 1958, SURG GYNECOL OBSTET, V107, P602
[7]   THE THORACOABDOMINAL SYNDROME (TAS) - A NEW X-LINKED DOMINANT DISORDER [J].
CARMI, R ;
BARBASH, A ;
MARES, AJ .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 36 (01) :109-114
[8]   SCHISIS-ASSOCIATION [J].
CZEIZEL, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 10 (01) :25-35
[9]   A 5-GENERATION FAMILY WITH SACRAL AGENESIS AND SPINA-BIFIDA - POSSIBLE SIMILARITIES WITH THE MOUSE T-LOCUS [J].
FELLOUS, M ;
BOUE, J ;
MALBRUNOT, C ;
WOLLMAN, E ;
SASPORTES, M ;
VANCONG, N ;
MARCELLI, A ;
REBOURCET, R ;
HUBERT, C ;
DEMENAIS, F ;
ELSTON, RC ;
NAMBOODIRI, KK ;
KAPLAN, EB ;
FELLOUS, M .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 12 (04) :465-487
[10]   CARDIAC AND NONCARDIAC MALFORMATIONS - OBSERVATIONS IN A POPULATION-BASED STUDY [J].
FERENCZ, C ;
RUBIN, JD ;
MCCARTER, RJ ;
BOUGHMAN, JA ;
WILSON, PD ;
BRENNER, JI ;
NEILL, CA ;
PERRY, LW ;
HEPNER, SI ;
DOWNING, JW .
TERATOLOGY, 1987, 35 (03) :367-378