{"id":1425212,"date":"2021-12-21T14:34:22","date_gmt":"2021-12-21T13:34:22","guid":{"rendered":"https:\/\/staging-wp-int.laboklin.com\/products\/genetics\/hereditary-diseases\/dog\/amelogenesis-imperfecta-familial-enamel-hypoplasia-feh\/"},"modified":"2021-12-21T14:34:22","modified_gmt":"2021-12-21T13:34:22","slug":"amelogenesis-imperfecta-familial-enamel-hypoplasia-feh","status":"publish","type":"page","link":"https:\/\/laboklin.com\/it\/esami\/genetica\/malattie-ereditarie\/dog\/amelogenesis-imperfecta-familial-enamel-hypoplasia-feh\/","title":{"rendered":"Amelogenesis imperfecta \/ Familial enamel hypoplasia (FEH)"},"content":{"rendered":"<h3 class=\"csc-firstHeader\">Amelogenesis imperfecta \/ Familial enamel hypoplasia (AI\/FEH)<\/h3><p><span>LABOKLIN Service ID: 8303<\/span><\/p><p class=\"bodytext\">Amelogenesis imperfecta (AI) or familial enamel hypoplasia (FEH) is an inherited condition of tooth enamel malformation. It is caused by a mutation in the ENAM or ACP4 gene which disrupts the production of Enamelin, an important component of tooth enamel. Affected animals have slim, pointed teeth with thin brown tooth enamel.<\/p><table class=\"tx-laboklinleistung-table contenttable contenttable-2\" style=\"margin-top: 35px;\"><tr><td class=\"td-0\"><strong>Method<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">TaqMan SNP assay (Akita, American Akita, Italian Greyhound);<br> sequencing (Parson Russell Terrier, Samoyed)<\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Breed list<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">Akita, American Akita, Italian Sighthound, Parson Russell Terrier, Samoyed<\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Heredity<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">autosomal recessive<\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Duration<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">3 - 5 days after arrival of the sample  in the lab (Akita, American Akita, Italian Greyhound);<br>\r\n1 - 2 weeks after arrival of the sample in the lab (Parson Russell Terrier, Samoyed)<\/p><\/td><\/tr><\/table>\n","protected":false},"excerpt":{"rendered":"<p>Amelogenesis imperfecta \/ Familial enamel hypoplasia (AI\/FEH)LABOKLIN Service ID: 8303Amelogenesis imperfecta (AI) or familial enamel hypoplasia (FEH) is an inherited condition of tooth enamel malformation. It is caused by a mutation in the ENAM or ACP4 gene which disrupts the production of Enamelin, an important component of tooth enamel. Affected animals have slim, pointed teeth&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1419947,"menu_order":5,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_robots_primary_cat":"","_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","footnotes":""},"class_list":["post-1425212","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/pages\/1425212","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/comments?post=1425212"}],"version-history":[{"count":0,"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/pages\/1425212\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/pages\/1419947"}],"wp:attachment":[{"href":"https:\/\/laboklin.com\/it\/wp-json\/wp\/v2\/media?parent=1425212"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}