{"id":1103,"date":"2016-03-17T23:19:27","date_gmt":"2016-03-17T23:19:27","guid":{"rendered":"https:\/\/www.primarycaregenetics.org\/?page_id=1103"},"modified":"2016-03-17T23:19:50","modified_gmt":"2016-03-17T23:19:50","slug":"netherlands","status":"publish","type":"page","link":"https:\/\/www.primarycaregenetics.org\/?page_id=1103&lang=nl","title":{"rendered":"Netherlands"},"content":{"rendered":"<div id=\"attachment_473\" style=\"width: 183px\" class=\"wp-caption alignleft\"><img aria-describedby=\"caption-attachment-473\" loading=\"lazy\" class=\"size-full wp-image-473\" src=\"https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/07\/IMG_3686-e1444942648931.jpg\" alt=\"SONY DSC\" width=\"173\" height=\"116\" \/><p id=\"caption-attachment-473\" class=\"wp-caption-text\">SONY DSC<\/p><\/div>\n<p>Peggy Rutten \u2013 praktijk ondersteuner Huisartsenpraktijk Maastricht<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>In English<\/p>\n<!--[if lt IE 9]><script>document.createElement('audio');<\/script><![endif]-->\n<audio class=\"wp-audio-shortcode\" id=\"audio-1103-1\" preload=\"none\" style=\"width: 100%;\" controls=\"controls\"><source type=\"audio\/mpeg\" src=\"https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/07\/Annett.mp3?_=1\" \/><a href=\"https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/07\/Annett.mp3\">https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/07\/Annett.mp3<\/a><\/audio>\n<p><img loading=\"lazy\" class=\"alignleft size-thumbnail wp-image-511\" src=\"https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/07\/image-300x269.jpg\" alt=\"image\" width=\"300\" height=\"269\" \/>My name is Annet Sollie and I am in General Practitioner in her final year of training. I have always been fascinated by genetics and when you have an eye for it, genetics is everywhere. I notice however, that many collegues in Primary Care are much less aware of genetics.<\/p>\n<p>In General Practice, almost every day I encounter patients where it is relevant to take a short family history. For instance, when someone experiences chest pain at a relatively young age or when a woman visits me with fear of breast cancer. This influences my referrals.<\/p>\n<p>Also when I see children with developmental delay, learning problems or dysmorphic features I do not hesitate to explore further or ask a paediatrican or clinical geneticist to advise me.<\/p>\n<p>In my opinion, it is a mindset; you have to be aware of things out of the ordinary. And of course, you have to develop the necessary skills such as taking a relevant family history.<\/p>\n<p>&nbsp;<\/p>\n<audio class=\"wp-audio-shortcode\" id=\"audio-1103-2\" preload=\"none\" style=\"width: 100%;\" controls=\"controls\"><source type=\"audio\/mpeg\" src=\"https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/08\/Netherlands.mp3?_=2\" \/><a href=\"https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/08\/Netherlands.mp3\">https:\/\/www.primarycaregenetics.org\/wp-content\/uploads\/2015\/08\/Netherlands.mp3<\/a><\/audio>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Peggy Rutten \u2013 praktijk ondersteuner Huisartsenpraktijk Maastricht &nbsp; &nbsp; In English My name is Annet Sollie and I am in General Practitioner in her final year of training. I have always been fascinated by genetics and when you have an eye for it, genetics is everywhere. I notice however, that many collegues in Primary Care are much less aware of genetics. In General Practice, almost every day I encounter patients where it is relevant to take a short family history. [&#8230;]<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":1055,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"template-fullwidth.php","meta":{"ngg_post_thumbnail":0},"_links":{"self":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/1103"}],"collection":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1103"}],"version-history":[{"count":1,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/1103\/revisions"}],"predecessor-version":[{"id":1105,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/1103\/revisions\/1105"}],"up":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/1055"}],"wp:attachment":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1103"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}