Schnitzler Syndrome, and the MEFV Gene Variant F.J. Nicolás-Sánchez, J.I. Aróstegui-Gorospe, J. Tarragona-Foradada, A. González-Barranquero

Identification of a novel heterozygous variant c.497g>a (p.gly166glu) in exon 5 of the sting1 gene as the causative factor of sting-associated vasculopathy with onset in infancy (SAVI): a case report M. Mansilla-Polo, D. Martín-Torregrosa, M. Saro-Buendía, B. Escutia-Muñoz, R. Botella-Estrada

Granulomatous Variant of Pigmented Purpura H. Hakenoshita, T. Yamamoto