Sapp Julie C, Turner Joyce T, van de Kamp Jiddeke M, van Dijk Fleur S, Lowry R Brian, Biesecker Leslie G
National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Am J Med Genet A. 2007 Dec 15;143A(24):2944-58. doi: 10.1002/ajmg.a.32023.
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.
我们报告了一系列7例患者,他们之前被诊断为变形综合征,但不符合该疾病已发表的诊断标准,且其自然病史与变形综合征不同。这种新认识的表型包括进行性、复杂性和混合性躯干血管畸形、脂肪组织失调、不同程度的脊柱侧弯以及骨骼结构增大但无进行性骨质过度生长。我们基于启发式方法将这种病症命名为先天性脂肪瘤过度生长、血管畸形和表皮痣(CLOVE综合征)。与变形综合征典型的骨骼畸形不同,CLOVE综合征的畸形仅在进行大手术或根治性手术后出现。在此,我们对比了CLOVE综合征与变形综合征的异同。