forgot password<\/a>\n <\/div>\n\n \n \n <\/div>\n <\/div>\n<\/div>\n\n","protected":false},"excerpt":{"rendered":"craniofacial dysostosis, also known as crouzon syndrome, is one of the craniosynostosis syndromes. it is characterized by craniosynostosis, maxillary hypoplasia, shallow orbits, and ocular proptosis. it is inherited in autosomal dominant fashion and may exhibit quite variable expression within families. a large number of cases represent new mutations which are thought to be related to advanced paternal age. the gene responsible for crouzon syndrome is fgfr2, a member of the fibroblast growth factor receptor group. among the mutations reported is c342y.<\/p>\n","protected":false},"author":10,"featured_media":0,"menu_order":0,"template":"","tags":[23],"class_list":["post-3789","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\/3789","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\/3789\/revisions"}],"wp:attachment":[{"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/media?parent=3789"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"\/\/www.iolishoes.com\/wp-json\/wp\/v2\/tags?post=3789"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}