forgot password<\/a>\n <\/div>\n\n \n \n <\/div>\n <\/div>\n<\/div>\n\n","protected":false},"excerpt":{"rendered":"atelosteogenesis type i is characterized by micromelia, facial changes, narrow chest, joint dislocations and absent fibula. the modes of inheritance are both sporadic and recessive with a mutation on the dtdst gene on chromosome 5 and it is a lethal condition. it is also known as giant cell chondrodysplasia and spondylo-humero-femoral dysplasia.<\/p>\n","protected":false},"author":10,"featured_media":0,"menu_order":0,"template":"","tags":[23],"class_list":["post-3768","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\/3768","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\/3768\/revisions"}],"wp:attachment":[{"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/media?parent=3768"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/tags?post=3768"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}