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一名存活的早产婴儿患有22三体综合征,合并先天性膈疝及胼胝体缺失。

Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant.

作者信息

Kim E H, Cohen R S, Ramachandran P, Mineta A K, Babu V R

机构信息

Department of Pediatrics, Santa Clara Valley Medical Center, San Jose, CA 95128.

出版信息

Am J Med Genet. 1992 Nov 1;44(4):437-8. doi: 10.1002/ajmg.1320440410.

Abstract

We report on a liveborn premature male with trisomy 22 who had multiple congenital anomalies, including congenital diaphragmatic hernia and absence of corpus callosum. He died of pulmonary hypoplasia associated with diaphragmatic hernia within 12 hours of age. Chromosome analysis by multiple banding techniques based on lymphocyte culture confirmed that he had trisomy 22. This may be the first report of congenital diaphragmatic hernia and isolated absence of corpus callosum associated with trisomy 22.

摘要

我们报告了一例患有22三体综合征的活产早产男婴,其患有多种先天性异常,包括先天性膈疝和胼胝体缺失。他在出生后12小时内死于与膈疝相关的肺发育不全。基于淋巴细胞培养的多种显带技术进行的染色体分析证实他患有22三体综合征。这可能是首例与22三体综合征相关的先天性膈疝和孤立性胼胝体缺失的报告。

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