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5号染色体缺失:当前认知与未来方向

5p deletions: Current knowledge and future directions.

作者信息

Nguyen Joanne M, Qualmann Krista J, Okashah Rebecca, Reilly AmySue, Alexeyev Mikhail F, Campbell Dennis J

出版信息

Am J Med Genet C Semin Med Genet. 2015 Sep;169(3):224-38. doi: 10.1002/ajmg.c.31444. Epub 2015 Aug 3.

Abstract

Disorders resulting from 5p deletions (5p-) were first recognized by Lejeune et al. in 1963 [Lejeune et al. (1963); C R Hebd Seances Acad Sci 257:3098-3102]. 5p- is caused by partial or total deletion of the short arm of chromosome 5. The most recognizable phenotype is characterized by a high-pitched cry, dysmorphic features, poor growth, and developmental delay. This report reviews 5p- disorders and their molecular basis. Hemizygosity for genes located within this region have been implicated in contributing to the phenotype. A review of the genes on 5p which may be dosage sensitive is summarized. Because of the growing knowledge of these specific genes, future directions to explore potential targeted therapies for individuals with 5p- are discussed. © 2015 Wiley Periodicals, Inc.

摘要

5号染色体短臂缺失(5p-)导致的疾病最早由勒热纳等人于1963年发现[勒热纳等人(1963年);《法国科学院院报》257:3098 - 3102]。5p-是由5号染色体短臂的部分或全部缺失引起的。最易识别的表型特征为高音调哭声、畸形面容、生长发育迟缓。本报告回顾了5p-相关疾病及其分子基础。该区域内基因的半合子状态被认为与表型形成有关。总结了5号染色体上可能对剂量敏感的基因。鉴于对这些特定基因的认识不断增加,还讨论了探索针对5p-个体潜在靶向治疗方法的未来方向。© 2015威利期刊公司

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