Parkes Weber syndrome, vein of galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations

Nicole Revencu, Laurence M. Boon, John B. Mulliken, Odile Enjolras, Maria Rosa Cordisco, Patricia E. Burrows, Philippe Clapuyt, Frank Hammer, Josée Dubois, Eulalia Baselga, Francesco Brancati, Robin Carder, José Miguel Ceballos Quintal, Bruno Dallapiccola, Gayle Fischer, Ilona J. Frieden, Maria Garzon, John Harper, Jennifer Johnson-Patel, Christine LabrèzeLoreto Martorell, Harriet J. Paltiel, Annette Pohl, Julie Prendiville, Isabelle Quere, Dawn H. Siegel, Enza Maria Valente, Annet Van Hagen, Liselot Van Hest, Keith K. Vaux, Asuncion Vicente, Lisa Weibel, David Chitayat, Miikka Vikkula

Research output: Contribution to journalArticlepeer-review

333 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)959-965
Number of pages7
JournalHuman mutation
Issue number7
StatePublished - Jul 2008


  • Arteriovenous
  • Arteriovenous fistula
  • Capillary
  • Hereditary benign telangiectasia
  • Hereditary hemorrhagic telangiectasia
  • Malformation
  • NF1
  • NF2
  • Parkes Weber syndrome
  • RAS p21
  • RASA1
  • p120RasGAP

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


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