DeSilva, MaliniMuñoz, Flor M.Sell, ErickMarshall, HelenTse Kawai, Alison TseKachikis, AlisaHeath, Paul T.Klein, Nicola P.Oleske, James M.Jehan, FyezahSpiegel, HansNesin, MirjanaTagbo, Beckie N.Shrestha, AnjuCutland, Clare L.Eckert, Linda O.Kochhar, SonaliBardají, AzucenaBrighton Collaboration Congenital Microcephaly Working Group2017-12-112017-12-112017-12-040264-410Xhttps://hdl.handle.net/2445/118599Need for developing case definitions and guidelines for data collection, analysis, and presentation for congenital microcephaly as an adverse event following maternal immunisation Congenital microcephaly, also referred to as primary microcephaly due to its presence in utero or at birth, is a descriptive term for a structural defect in which a fetus or infant’s head (cranium) circumference is smaller than expected when compared to other fetuses or infants of the same gestational age, sex and ethnic background.11 p.application/pdfengcc by (c) Elsevier, 2017http://creativecommons.org/licenses/by/3.0/es/Malalties cerebralsMalalties hereditàriesBrain diseasesGenetic diseasesCongenital microcephaly: Case definition & guidelines for data collection, analysis, and presentation of safety data after maternal immunisationinfo:eu-repo/semantics/article2017-12-06info:eu-repo/semantics/openAccess29150052