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These forms have been named with numbers, eponyms or descriptive names. Some of these syndromes can actually be considered congenital forms of brittle bones resembling OI (SROI).<\/jats:p>\n                     <\/jats:sec><jats:sec>\n                        <jats:title>Discussion<\/jats:title>\n                        <jats:p>A review of different syndromes with congenital brittle bones published in the literature is presented. Syndromes are classified in \"OI\" (those secondary to mutations in the type I pro-collagen genes), and \"syndromes resembling OI\" (those secondary to mutations other that the type I pro-collagen genes, identified or not). A definition for OI is proposed as a syndrome of congenital brittle bones secondary to mutations in the genes codifying for pro-collagen genes (COL1A1 and COL1A2).<\/jats:p>\n                     <\/jats:sec><jats:sec>\n                        <jats:title>Summary<\/jats:title>\n                        <jats:p>A debate about the definition of OI and a possible clinical and prognostic classification are warranted.<\/jats:p>\n                     <\/jats:sec>","DOI":"10.1186\/1471-2431-4-16","type":"journal-article","created":{"date-parts":[[2004,9,2]],"date-time":"2004-09-02T13:05:12Z","timestamp":1094130312000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":48,"title":["Syndromes with congenital brittle bones"],"prefix":"10.1186","volume":"4","author":[{"given":"Horacio","family":"Plotkin","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2004,8,31]]},"reference":[{"key":"43_CR1","first-page":"233","volume":"75","author":"R Smith","year":"1994","unstructured":"Smith R: Osteogenesis imperfecta: from phenotype to genotype and back again. 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