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一名22号染色体部分三体综合征患者的肋椎发育异常。

Costovertebral dysplasia in a patient with partial trisomy 22.

作者信息

Tonk Vijay, Wilson Golder, Schutt Robert, Mock Justin, Wyandt Herman, Mark Hon Fong L, Ito Masamichi

机构信息

Department of Pediatrics, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.

出版信息

Exp Mol Pathol. 2006 Apr;80(2):197-200. doi: 10.1016/j.yexmp.2005.08.011. Epub 2005 Nov 2.

Abstract

A newborn female presented with costovertebral dysplasia (CVD), subtle facial anomalies, and neonatal respiratory distress. Her karyotype demonstrated a small supernumerary NOR-positive marker that was subsequently identified as del(22)(q11.2). This extra structurally abnormal chromosome was found by DNA microsatellite marker analyses to be derived from a paternal chromosome 22. The child has had severe growth and developmental delay along with pulmonary insufficiency and hypoxia but is presently stable at age 20 months. Findings in our patient correlate with similar observations in children with small markers derived from D/G and D/D translocations reported before banding technology was available. These reports and recent mapping results suggest that a pericentric gene family, distributed on one or more acrocentric chromosomes, may have played a role in the development of the human axial skeleton. Data from additional studies will be needed to confirm or refute this hypothesis.

摘要

一名新生女婴表现出肋椎发育不良(CVD)、细微的面部异常和新生儿呼吸窘迫。她的核型显示有一个小的额外核仁组织区(NOR)阳性标记,随后被鉴定为22号染色体长臂1区2带缺失(del(22)(q11.2))。通过DNA微卫星标记分析发现,这条额外的结构异常染色体来自父源22号染色体。该患儿有严重的生长和发育迟缓,伴有肺功能不全和缺氧,但目前在20个月大时情况稳定。我们患者的发现与在带型技术出现之前报道的来自D/G和D/D易位的小标记患儿的类似观察结果相关。这些报告和最近的定位结果表明,一个分布在一条或多条近端着丝粒染色体上的着丝粒周围基因家族可能在人类中轴骨骼的发育中起了作用。需要更多研究的数据来证实或反驳这一假设。

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