The Hunter-McAlpine syndrome results from duplication 5q35-qter

被引:15
作者
Hunter, AGW
Dupont, B
McLaughlin, M
Hinton, L
Baker, E
Adès, L
Haan, E
Schwart, CE
机构
[1] Greenwood Genet Ctr, Greenwood, SC 29646 USA
[2] Reg Genet Program Eastern Ontario, Ottawa, ON, Canada
[3] Womens & Childrens Hosp, Dept Genet Med, Adelaide, SA, Australia
[4] Univ Adelaide, Dept Paediat, Adelaide, SA, Australia
关键词
chromosome paint; cryptic translocation; Hunter-McAlpine syndrome; subtelomeric probes;
D O I
10.1111/j.1399-0004.2005.00378.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In 1977 Hunter et al. J Med Genet 1977: 14 (6): 430-437. reported a family with six affected members, connected over three generations through unaffected individuals. Subsequently, several other patients purported to have the condition were reported. The condition became known as the Hunter-McAlpine syndrome, and there was debate as to whether or not it was identical to the Ruvalcaba syndrome or a type of tricho-rhino-phalangeal syndrome. In this article we confirm that the original family and a patient reported by Ades et al. Clin Dysmorphol 1993: 2 (2): 123-130 have cryptic translocations resulting in duplication of 5q35-qter. Similarities are noted between our patients and others in the literature with duplication of this chromosome segment.
引用
收藏
页码:53 / 60
页数:8
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