{"id":522,"date":"2018-05-04T15:24:12","date_gmt":"2018-05-04T15:24:12","guid":{"rendered":"https:\/\/simonsvipcms.wordpress.com\/?page_id=522"},"modified":"2025-01-29T14:25:02","modified_gmt":"2025-01-29T19:25:02","slug":"kdm6b","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/kdm6b\/","title":{"rendered":"KDM6B"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The information for this summary of <\/span><strong><span class=\"notranslate\">KDM6B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> comes from research publications. This is not meant to take the place of medical advice.<\/span><\/p>\n<p><a href=\"https:\/\/www.simonssearchlight.org\/gene-guide\/kdm6b\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here for our full KDM6B Gene Guide<\/strong><\/a><\/p>\n<p><span style=\"font-weight: 400;\">The online Gene Guide includes more information about <span class=\"notranslate\">KDM6B<\/span> such as the chance of having another child with this condition, behavior and development concerns linked to <span class=\"notranslate\">KDM6B<\/span>-related syndrome or specialists to consider for people with this condition. Share this resource with family members or your clinical providers.<\/span><\/p>\n<p><strong><span class=\"notranslate\">KDM6B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> is also called <\/span><strong>Stolerman neurodevelopmental syndrome, neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities (NEDCFSA), and <span class=\"notranslate\">KDM6B<\/span>-related neurodevelopmental disorder<\/strong><span style=\"font-weight: 400;\">.<\/span> <span style=\"font-weight: 400;\">For this webpage, we will be using the name <\/span><strong><span class=\"notranslate\">KDM6B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> to encompass the wide range of variants observed in the people identified.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The information for this summary of KDM6B-related syndrome comes from research publications. This is not meant to take the place of medical advice. Click here for our full KDM6B Gene Guide The online Gene Guide includes more information about KDM6B such as the chance of having another child with this condition, behavior and development concerns [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":0,"parent":29,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-gene-card.php","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"acf":[],"_links":{"self":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/522"}],"collection":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=522"}],"version-history":[{"count":43,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/522\/revisions"}],"predecessor-version":[{"id":59258,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/522\/revisions\/59258"}],"up":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/29"}],"wp:attachment":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/media?parent=522"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}