Urreizti, RoserGrinberg Vaisman, Daniel RaúlBalcells Comas, Susana2024-03-182024-03-182019-03-022167-8707https://hdl.handle.net/2445/208921In 1969 Opitz et al. described two siblings with a new syndrome, which they called ‘C syndrome of multiple congenital abnormalities’ and was presented as a ‘probably private syndrome’. After this first description, new cases appeared with highly similar phenotypes and a new syndrome, known as C Syndrome, Opitz C Syndrome or Opitz Trigonocephaly Syndrome (OCS; MIM # 211,750) was firmly established.4 p.application/pdfeng(c) Taylor & Francis, 2019CraniDiagnòsticMalformacionsSkullDiagnosisHuman abnormalitiesC syndrome - what do we know and what could the future hold?info:eu-repo/semantics/article6875102024-03-18info:eu-repo/semantics/openAccess