Licciardi, FrancescoMontin, DavideVersace, AntoniaMigliore, GiuseppinaTzialla, ChryssoulaFellay, JacquesBorghesi, Alessandro2017-01-242017-01-242017-01-24201610.1016/j.ijid.2016.08.010https://infoscience.epfl.ch/handle/20.500.14299/133771WOS:000388326700006Two cases of neonatal group B streptococcal (GBS) infection occurring in a large consanguineous kindred are described. The observation suggests that susceptibility to isolated GBS disease in this family may have been the result of an inborn error of immunity inherited as a Mendelian autosomal recessive trait. (C) 2016 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license.Streptococcus agalactiaeGBSNeonatalGeneticPrimary immunodeficiencyMendeliantext::journal::journal article::research article