Constitutional mosaicism in RASA1-related capillary malformation-arteriovenous malformation

Clin Genet. 2019 Apr;95(4):516-519. doi: 10.1111/cge.13499. Epub 2019 Feb 4.

Abstract

Capillary malformation-arteriovenous malformation (CM-AVM) is caused by germline RASA1 and EPHB4 alterations. RASA1 intralesional second hits have also been reported. Here we report RASA1 constitutional mosaicism, defined here as the presence of a mosaic variant in all cell types of an individual, in two patients with CM-AVM. High-throughput sequencing was used to search for RASA1 pathogenic variants in blood samples from two unrelated patients with CM-AVM. An affected tissue sample from one of the patients was also analyzed. Both patients showed different nonsense RASA1 variants in mosaic, ranging from 7% to 21.5%, in blood samples and in the corresponding affected tissue sample from one of the patients. In conclusion, we report for the first time the presence of RASA1 constitutional mosaicism in CM-AVM. Constitutional mosaicism has implications for accurate molecular diagnosis and recurrence risk and helps to explain the great phenotypic variability in CM-AVM.

Keywords: RASA1; capillary malformation-arteriovenous malformation; constitutional mosaicism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acid Substitution
  • Arteriovenous Malformations / diagnosis*
  • Arteriovenous Malformations / genetics*
  • Capillaries / abnormalities*
  • Computed Tomography Angiography
  • Female
  • Genetic Association Studies* / methods
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Male
  • Mosaicism*
  • Mutation*
  • Port-Wine Stain / diagnosis*
  • Port-Wine Stain / genetics*
  • p120 GTPase Activating Protein / genetics*

Substances

  • RASA1 protein, human
  • p120 GTPase Activating Protein

Supplementary concepts

  • Capillary Malformation-Arteriovenous Malformation