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