Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients

被引:154
作者
Sapp, Julie C.
Turner, Joyce T.
van de Kamp, Jiddeke M.
van Dijk, Fleur S.
Lowry, R. Brian
Biesecker, Leslie G.
机构
[1] NHGRI, NIH, Bethesda, MD 20892 USA
[2] Vrije Univ Amsterdam, VU Univ Med Ctr, Amsterdam, Netherlands
[3] Univ Calgary, Dept Med Genet, Calgary, AB, Canada
[4] Alberta Childrens Prov Gen Hosp, Calgary, AB T2T 5C7, Canada
关键词
overgrowth; asymmetric overgrowth; hemihyperplasia; bone distortion; Proteus syndrome; hemihyperplasia-multiple lipomatosis syndrome (HHML); Klippel-Trenaunay syndrome;
D O I
10.1002/ajmg.a.32023
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
We present a series of seven patients who were previously diagnosed with Proteus syndrome, but who do not meet published diagnostic criteria for this disorder and whose natural history is distinct from that of Proteus syndrome. This newly recognized phenotype comprises progressive, complex, and mixed truncal vascular malformations, dysregulated adipose tissue, varying degrees of scoliosis, and enlarged bony structures without progressive bony overgrowth. We have named this condition congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) on a heuristic basis. in contrast to the bony distortion so characteristic of Proteus syndrome, distortion in CLOVE syndrome occurs only following major or radical surgery. Here, we contrast differences and similarities of CLOVE syndrome to Proteus syndrome. (C) 2007 Wiley-Liss, Inc.
引用
收藏
页码:2944 / 2958
页数:15
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