Brachmann-de Lange syndrome with congenital diaphragmatic hernia and NIPBL gene mutation

被引:14
|
作者
Hosokawa, Shinichi [1 ]
Takahashi, Nobumasa [1 ]
Kitajima, Hiroyuki [1 ]
Nakayama, Masahiro [2 ]
Kosaki, Kenjirou [3 ]
Okamoto, Nobuhiko [4 ,5 ]
机构
[1] Keio Univ, Sch Med, Dept Neonatol, Osaka, Japan
[2] Keio Univ, Sch Med, Dept Pathol, Osaka, Japan
[3] Keio Univ, Sch Med, Dept Pediat, Osaka, Japan
[4] Keio Univ, Sch Med, Dept Dev Pediat, Osaka Med Ctr, Osaka, Japan
[5] Keio Univ, Sch Med, Res Inst Maternal & Child Hlth, Osaka, Japan
关键词
Brachmann-de Lange syndrome; congenital diaphragmatic hernia; denaturing high-performance liquid chromatography; direct sequence method; gene mutation; GENOTYPE-PHENOTYPE CORRELATIONS; DELANGE-SYNDROME; NIPPED-B; HOMOLOG;
D O I
10.1111/j.1741-4520.2010.00270.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We report herein a case of Brachmann-de Lange syndrome complicated with congenital diaphragmatic hernia in which a NIPBL gene mutation was identified. A female infant born at 37 weeks of gestation died 134 min after delivery, even though endotracheal intubation and resuscitation were performed immediately after the scheduled caesarean operation. We diagnosed the infant with Brachmann-de Lange syndrome from her physical characteristics. An abnormal peak at the 29th exon in the translation area of the NIPBL gene was detected using denaturing high-performance liquid chromatography. In addition, a mutation of cytosine to thymine (nonsense mutation) at the 5524th base was identified using the direct sequence method. This variation was likely the cause of the syndrome.
引用
收藏
页码:129 / 132
页数:4
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