DNA methylation alterations in the genome of a toddler with cri-du-chat syndrome

被引：3
|
作者：
Naumova, Oxana Y. [1 ,2 ]
Rychkov, Sergey Y. [2 ]
Kuznetzova, Tatyana V. [3 ]
Odintsova, Veronika V. [4 ]
Kornilov, Sergey A. [1 ,4 ]
Grigorenko, Elena L. [1 ,4 ]
机构：
[1] Univ Houston, Texas Inst Measurement Evaluat & Stat, 4849 Calhoun Rd, Houston, TX 77204 USA
[2] RAS, Vavilov Inst Gen Genet, Lab Human Genet, Moscow, Russia
[3] DO Otts Res Inst Obstet Gynecol & Reproductol, St Petersburg, Russia
[4] St Petersburg State Univ, Dept Psychol, St Petersburg, Russia
来源：
CLINICAL CASE REPORTS | 2018年 / 6卷 / 01期
关键词：
case study; cri-du-chat syndrome; DNA methylation; Illumina Infinium Human Methylation450;
D O I：
10.1002/ccr3.1274
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
This manuscript reports on genomewide epigenetic alterations in cri-du-chat syndrome related to a partial aneusomy of chromosome 5. A systematic analysis of these alterations will open up new possibilities for the prognostic evaluation of CDCS patients and the development of new therapeutic interventions for reducing the severity of the disease.
引用
收藏
页码：14 / 17
页数：4
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