{"id":6525,"date":"2024-11-07T15:19:25","date_gmt":"2024-11-07T15:19:25","guid":{"rendered":"https:\/\/edren.org\/ren\/?page_id=6525"},"modified":"2024-11-07T15:19:25","modified_gmt":"2024-11-07T15:19:25","slug":"alport-spectrum","status":"publish","type":"page","link":"https:\/\/edren.org\/ren\/edren-info\/alport-syndrome\/alport-spectrum\/","title":{"rendered":"Alport spectrum"},"content":{"rendered":"<p>It is now known that about 1 in 100 people carry an Alport gene variant (&#8216;mutation&#8217;) that could cause disease, but it is inherited with a second normal copy. While most people who have this remain well, a minority do develop kidney disease. The lifetime risk of developing kidney disease is definitely increased, but only a small minority run into serious trouble, and it us usually (but not always) in later life.<\/p>\n<p>We need to learn more about what makes kidney disease more likely in people with this &#8211; is it other genes you inherit, or things that happen to you?<\/p>\n<p>This has led to the concept of a spectrum of Alport-related disease. It overlaps with <a href=\"https:\/\/edren.org\/ren\/edren-info\/glomerular-basement-membrane-disorders\/\">Thin Basement Membrane<\/a> Nephropathy\/Disease. See figure below.<\/p>\n<p>Figure:<\/p>\n","protected":false},"excerpt":{"rendered":"<p>It is now known that about 1 in 100 people carry an Alport gene variant (&#8216;mutation&#8217;) that could cause disease, but it is inherited with a second normal copy. While most people who have this remain well, a minority do develop kidney disease. The lifetime risk of developing kidney disease\u2026<\/p>\n<p> <a class=\"continue-reading-link\" href=\"https:\/\/edren.org\/ren\/edren-info\/alport-syndrome\/alport-spectrum\/\"><span>Continue reading<\/span><i class=\"crycon-right-dir\"><\/i><\/a> <\/p>\n","protected":false},"author":1,"featured_media":0,"parent":227,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"class_list":["post-6525","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/pages\/6525","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/comments?post=6525"}],"version-history":[{"count":1,"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/pages\/6525\/revisions"}],"predecessor-version":[{"id":6526,"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/pages\/6525\/revisions\/6526"}],"up":[{"embeddable":true,"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/pages\/227"}],"wp:attachment":[{"href":"https:\/\/edren.org\/ren\/wp-json\/wp\/v2\/media?parent=6525"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}