EXTRAHEPATIC BILIARY ATRESIA AND ASSOCIATED ANOMALIES - ETIOLOGIC HETEROGENEITY SUGGESTED BY DISTINCTIVE PATTERNS OF ASSOCIATIONS

被引:74
作者
CARMI, R
MAGEE, CA
NEILL, CA
KARRER, FM
机构
[1] UNIV MARYLAND,DEPT EPIDEMIOL & PREVENT MED,655 W BALTIMORE ST,BALTIMORE,MD 21201
[2] BEN GURION UNIV NEGEV,SOROKA MED CTR,CLIN GENET UNIT,IL-84105 BEER SHEVA,ISRAEL
[3] UNIV MARYLAND,DIV HUMAN GENET,BALTIMORE,MD 21201
[4] JOHNS HOPKINS UNIV,SCH MED,DIV PEDIAT CARDIOL,BALTIMORE,MD 21205
[5] UNIV COLORADO,SCH MED,DEPT SURG,DENVER,CO 80202
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 45卷 / 06期
关键词
EXTRAHEPATIC BILIARY ATRESIA; LATERALITY SEQUENCE; SITUS INVERSUS; POLYSPLENIA; ASSOCIATED ANOMALIES;
D O I
10.1002/ajmg.1320450606
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fifty-one cases of extrahepatic biliary atresia (EHBA) with associated anomalies were found in a study of EHBA (251 cases). Analysis of segregation patterns of these anomalies in individual patients suggested the existence of 2 major groups: (1) 15 cases (29.4%) with various combinations of anomalies within the laterality sequence, and (2) 30 cases (58.8%) with one or 2 anomalies mostly involving the cardiac, gastrointestinal, and urinary systems. These latter anomalies did not follow any recognizable pattern. The third group of 6 cases all had intestinal malrotation, some with preduodenal portal vein; these cases show some similarity to the laterality sequence group and may represent a more confined phenotypic result of faulty situs determination. This previously unattempted classification of patients with EHBA and associated anomalies might enable a more targeted approach towards identification of causes in this heterogeneous disorder. EHBA within the laterality sequence might prove a suitable candidate for a major gene mutation. Teratogenic, infectious and polygenic multifactorial causes might play a more significant role in EHBA associated with ''nonsyndromic'' organ system anomalies.
引用
收藏
页码:683 / 693
页数:11
相关论文
共 90 条
[1]   BILIARY ATRESIA AND NONCARDIAC POLYSPLENIC SYNDROME - US AND SURGICAL CONSIDERATIONS [J].
ABRAMSON, SJ ;
BERDON, WE ;
ALTMAN, RP ;
AMODIO, JB ;
LEVY, J .
RADIOLOGY, 1987, 163 (02) :377-379
[2]   PROBABLE AUTOSOMAL RECESSIVE INHERITANCE OF POLYSPLENIA, SITUS INVERSUS AND CARDIAC DEFECTS IN AN AMISH FAMILY [J].
ARNOLD, GL ;
BIXLER, D ;
GIROD, D .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 16 (01) :35-42
[3]   LINKAGE MAPPING OF A MOUSE GENE, IV, THAT CONTROLS LEFT RIGHT ASYMMETRY OF THE HEART AND VISCERA [J].
BRUECKNER, M ;
DEUSTACHIO, P ;
HORWICH, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :5035-5038
[4]  
BRUN P, 1985, ANN RADIOL, V28, P259
[5]  
CAMPBELL M, 1967, BRIT HEART J, V29, P268
[6]  
CARMI R, 1991, UNPUB BALTIMORE WASH
[7]   DUCTAL REMNANTS IN EXTRA-HEPATIC BILIARY ATRESIA - HISTOPATHOLOGIC STUDY WITH CLINICAL CORRELATION [J].
CHANDRA, RS ;
ALTMAN, RP .
JOURNAL OF PEDIATRICS, 1978, 93 (02) :196-200
[8]   BILIARY ATRESIA AND OTHER STRUCTURAL ANOMALIES IN CONGENITAL POLYSPLENIA SYNDROME [J].
CHANDRA, RS .
JOURNAL OF PEDIATRICS, 1974, 85 (05) :649-655
[9]   VARIATION IN THE COURSE OF VESSELS IN THE VICINITY OF THE HEPATIC PORT IN BILIARY ATRESIA [J].
CHIBA, T ;
KASAI, M ;
SUZUKI, T .
JOURNAL OF PEDIATRIC SURGERY, 1987, 22 (10) :963-966
[10]  
CZEIZEL A, 1987, Acta Paediatrica Hungarica, V28, P63