Clinical report - Prenatal diagnosis of partial trisomy 1q and monosomy X in a fetus with a congenital lung lesion and hydrops fetalis

被引:10
作者
Pressey, Tracy L.
Wilson, R. Douglas
Kasperski, Stefanie
Bebbington, Michael W.
Adzick, N. Scott
机构
[1] Univ Penn, Ctr Fetal Diag & Treatment, Childrens Hosp Philadelphia, Dept Surg, Philadelphia, PA 19104 USA
[2] Univ British Columbia, Dept Obstet & Gynecol, Div Maternal Fetal Med, Vancouver, BC V5Z 1M9, Canada
关键词
congenital cystic adenomatoid malformation of lung; chromosome; 1; chromosome X; genetic translocation; prenatal diagnosis; hydrops fetalis;
D O I
10.1002/ajmg.a.31707
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on the prenatal diagnosis of partial trisomy 1q and monosomy X in a fetus with a congenital lung lesion and hydrops. The finding of hydrops in a fetus with a small lung lesion, congenital cystic adenomatoid malformation (CCAM) volume to head circumference ratio (CVR) 0.78, prompted cytogenetic analysis of amniotic fluid, revealing an unbalanced translocation between chromosomes X and 1[46,X,der(X)t(X;1)(p11.2;q25 or q31)]. The incidence of chromosomal abnormalities with CCAM lesions is estimated at 1.6%. This is the first reported case of prenatally diagnosed partial trisomy 1q and monosomy X presenting as a fetal lung lesion and hydrops. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1104 / 1107
页数:4
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