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 caused by abnormalities in type i collagen. it is characterized by bone fragility, osteopenia and progressive skeletal deformities. associated features in some individuals include blue sclerae, dentinogenesis imperfecta, hearing loss, deformity of the spine and long bones and joint hyperextensibility. it is characterized by marked inter- and intra-familial variability, making prenatal diagnosis difficult even in families with an established diagnosis. <\/p>\n","protected":false},"author":10,"featured_media":0,"menu_order":0,"template":"","tags":[23],"class_list":["post-3846","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\/3846","targethints":{"allow":["get"]}}],"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\/3846\/revisions"}],"wp:attachment":[{"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/media?parent=3846"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/tags?post=3846"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}