Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes

被引:86
作者
Delnatte, Capucine
Sanlaville, Damien
Mougenot, Jean-Francois
Vermeesch, Joris-Robert
Houdayer, Claude
de Blois, Marie-Christine
Genevieve, David
Goulet, Olivier
Fryns, Jean-Pierre
Jaubert, Francis
Vekemans, Michel
Lyonnet, Stanislas
Romana, Serge
Eng, Charis
Stoppa-Lyonnet, Dominique
机构
[1] Inst Curie, Dept Genet, Paris, France
[2] Hop Necker Enfants Malad, AP HP, Dept Genet, Paris, France
[3] Hop Necker Enfants Malad, AP HP, Dept Pediat, Paris, France
[4] Hop Necker Enfants Malad, AP HP, Dept Pathol, Paris, France
[5] INSERM, E0210, Equipe Mixte, Paris, France
[6] Katholieke Univ Leuven, Ctr Human Genet, Louvain, Belgium
[7] Case Western Reserve Univ, Sch Med, Cleveland Clin, Genom Med Inst, Cleveland, OH 44106 USA
[8] Case Western Reserve Univ, Sch Med, Dept Genet, Cleveland, OH 44106 USA
关键词
D O I
10.1086/504301
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe four unrelated children who were referred to two tertiary referral medical genetics units between 1991 and 2005 and who are affected with juvenile polyposis of infancy. We show that these children are heterozygous for a germline deletion encompassing two contiguous genes, PTEN and BMPR1A. We hypothesize that juvenile polyposis of infancy is caused by the deletion of these two genes and that the severity of the disease reflects cooperation between these two tumor-suppressor genes.
引用
收藏
页码:1066 / 1074
页数:9
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