Mild Phenotype in a Patient With Mosaic del(8p)/inv dup del(8p)

被引:12
|
作者
Hand, Matthew
Gray, Carolyn [2 ]
Glew, Gwen [1 ]
Tsuchiya, Karen D. [2 ,3 ]
机构
[1] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[2] Seattle Childrens Hosp, Dept Labs, Seattle, WA USA
[3] Univ Washington, Sch Med, Dept Lab Med, Seattle, WA 98195 USA
关键词
inverted duplication; mosaicism; DNA array; 8p; INVERTED DUPLICATION; SHORT ARM; 8P; CHROMOSOME-8; DELETION; 8P23.1; REARRANGEMENT; REGION; GENE;
D O I
10.1002/ajmg.a.33669
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a female with a mild phenotype who is mosaic for two cell lines with different structural abnormalities of 8p, both resulting in large genomic imbalances. Molecular cytogenetic and G-banded chromosome analyses demonstrated that one cell line has a large terminal 8p deletion, with a breakpoint in 8p21.2. The other cell line contains a derivative chromosome 8, known as an inv dup del(8p) in the literature. This female has developmental delay, but lacks congenital anomalies that are associated with either 8p abnormality in non-mosaic form. The attenuated phenotype in this individual may be due to compensation of one cell line for imbalances in the other cell line. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:2827 / 2831
页数:5
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