Complex cytogenetic rearrangement of chromosome 8q in a case of Ambras syndrome

被引:0
|
作者
Tadin, M
Braverman, E
Cianfarani, S
Sobrino, AJ
Levy, B
Christiano, AM
Warburton, D
机构
[1] Columbia Univ, Dept Genet & Dev, New York, NY USA
[2] Columbia Univ, Dept Dermatol, New York, NY 10027 USA
[3] Columbia Univ, Dept Pediat, New York, NY 10027 USA
[4] Univ Rome Tor Vergata, Dept Pediat & Publ Hlth, Rome, Italy
[5] New York Presbyterian Hosp, Columbia Presbyterian Ctr, New York, NY USA
[6] CUNY Mt Sinai Sch Med, Dept Human Genet, New York, NY 10029 USA
[7] CUNY Mt Sinai Sch Med, Dept Pediat, New York, NY 10029 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 102卷 / 01期
关键词
Ambras syndrome; hair follicle; hypertrichosis; chromosome; 8; deletion; FISH;
D O I
10.1002/1096-8628(20010722)102:1<100::AID-AJMG1396>3.0.CO;2-O
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ambras syndrome (AMS) is a unique form of congenital universal hypertrichosis, The syndrome has been found in association with rearrangements of chromosome 8 in two isolated cases. One of these patients was reported to have an apparently balanced paracentric inversion of chromosome 8, inv(8)(q12q22). Our cytogenetic analysis on this patient showed that the rearrangement of chromosome 8 is more complex than initially reported. We detected an insertion of the q23-q24 region into a more proximal region of the long arm of chromosome 8 as well as a large deletion in 8q23:46,XX, rea(8)(8pter-->8q13::8q23.2-->8q24.1::8q13-->8q23.1::8q24.1-->8qter). Given the large number of breakpoints and the presence of a substantial deletion, it is surprising that the proposita did not show anomalies other than these characteristic of Ambras syndrome, (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:100 / 104
页数:5
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