Revencu Nicole, Boon Laurence M, Mulliken John B, Enjolras Odile, Cordisco Maria Rosa, Burrows Patricia E, Clapuyt Philippe, Hammer Frank, Dubois Josée, Baselga Eulalia, Brancati Francesco, Carder Robin, Quintal José Miguel Ceballos, Dallapiccola Bruno, Fischer Gayle, Frieden Ilona J, Garzon Maria, Harper John, Johnson-Patel Jennifer, Labrèze Christine, Martorell Loreto, Paltiel Harriet J, Pohl Annette, Prendiville Julie, Quere Isabelle, Siegel Dawn H, Valente Enza Maria, Van Hagen Annet, Van Hest Liselot, Vaux Keith K, Vicente Asuncion, Weibel Lisa, Chitayat David, Vikkula Miikka
Laboratory of Human Molecular Genetics, de Duve Institute, Université catholique de Louvain, Brussels, Belgium.
Hum Mutat. 2008 Jul;29(7):959-65. doi: 10.1002/humu.20746.
Capillary malformation-arteriovenous malformation (CM-AVM) is a newly recognized autosomal dominant disorder, caused by mutations in the RASA1 gene in six families. Here we report 42 novel RASA1 mutations and the associated phenotype in 44 families. The penetrance and de novo occurrence were high. All affected individuals presented multifocal capillary malformations (CMs), which represent the hallmark of the disorder. Importantly, one-third had fast-flow vascular lesions. Among them, we observed severe intracranial AVMs, including vein of Galen aneurysmal malformation, which were symptomatic at birth or during infancy, extracranial AVM of the face and extremities, and Parkes Weber syndrome (PKWS), previously considered sporadic and nongenetic. These fast-flow lesions can be differed from the other two genetic AVMs seen in hereditary hemorrhagic telangiectasia (HHT) and in phosphatase and tensin homolog (PTEN) hamartomatous tumor syndrome. Finally, some CM-AVM patients had neural tumors reminiscent of neurofibromatosis type 1 or 2. This is the first extensive study on the phenotypes associated with RASA1 mutations, and unravels their wide heterogeneity.
毛细血管畸形 - 动静脉畸形(CM - AVM)是一种新发现的常染色体显性遗传病,六个家族中的RASA1基因突变导致了该病。在此,我们报告了44个家族中的42个新的RASA1突变及其相关表型。其外显率和新发发生率都很高。所有受影响个体均表现为多灶性毛细血管畸形(CM),这是该疾病的标志。重要的是,三分之一的患者有快速血流性血管病变。其中,我们观察到严重的颅内动静脉畸形,包括大脑大静脉动脉瘤样畸形,这些在出生时或婴儿期就有症状,还有面部和四肢的颅外动静脉畸形以及帕克斯·韦伯综合征(PKWS),此前认为这些是散发性且非遗传性的。这些快速血流性病变可与遗传性出血性毛细血管扩张症(HHT)和磷酸酶及张力蛋白同源物(PTEN)错构瘤综合征中所见的另外两种遗传性动静脉畸形相区别。最后,一些CM - AVM患者有类似于1型或2型神经纤维瘤病的神经肿瘤。这是首次对与RASA1突变相关的表型进行的广泛研究,并揭示了它们广泛的异质性。