CHROMOSOME-7P - SYNDROME - CRANIOSYNOSTOSIS WITH PRESERVATION OF REGION-7P2

被引:22
作者
AUGHTON, DJ
CASSIDY, SB
WHITEMAN, DAH
DELACH, JA
GUTTMACHER, AE
机构
[1] UNIV ARIZONA,DEPT PEDIAT,GENET DYSMORPHOL SECT,TUCSON,AZ 85721
[2] UNIV CONNECTICUT,DEPT PEDIAT,DIV HUMAN GENET,FARMINGTON,CT 06032
[3] UNIV VERMONT,COLL MED,DEPT PEDIAT,BURLINGTON,VT 05405
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 40卷 / 04期
关键词
CHROMOSOME-7; DEL(7P); CRANIOSYNOSTOSIS; MULTIPLE CONGENITAL ANOMALIES;
D O I
10.1002/ajmg.1320400412
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Deletion of a portion of the short arm of chromosome 7 is associated with a recognizable phenotype which often includes craniosynostosis. Recent reports have suggested that craniosynostosis occurs only if there is a deletion involving band 7p21 or the segment distal to that band. We report on a boy who had an interstitial deletion of 7p, not involving band 7p21 or the segment distal to that band, who nevertheless had craniosynostosis. Thus, it appears that the determination of craniosynostosis in this syndrome is more complicated than has been suggested previously.
引用
收藏
页码:440 / 443
页数:4
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