forgot password<\/a>\n <\/div>\n\n \n \n <\/div>\n <\/div>\n<\/div>\n\n","protected":false},"excerpt":{"rendered":"osteogenesis imperfecta (oi) is a clinically and genetically heterogeneous group of inherited disorders of connective tissue, frequently of collagen type i, characterized by bone fragility. associated features in some individuals include blue sclerae, dentinogenesis imperfecta, hearing loss, deformity of the spine and long bones and joint hyperextensibility. the disorder is currently categorized into 4 major types, according to the phenotypic classification of sillence. there are several sub-types as well as marked heterogeneity at the clinical, radiological and molecular level within these groups. <\/p>\n","protected":false},"author":10,"featured_media":0,"menu_order":0,"template":"","tags":[23],"class_list":["post-3843","x5_anomaly_database","type-x5_anomaly_database","status-publish","hentry","tag-obstetric"],"_links":{"self":[{"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/x5_anomaly_database\/3843"}],"collection":[{"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/x5_anomaly_database"}],"about":[{"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/types\/x5_anomaly_database"}],"author":[{"embeddable":true,"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/users\/10"}],"version-history":[{"count":0,"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/x5_anomaly_database\/3843\/revisions"}],"wp:attachment":[{"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/media?parent=3843"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/tags?post=3843"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}