{"id":3693,"date":"2022-11-05T18:28:10","date_gmt":"2022-11-05T18:28:10","guid":{"rendered":"https:\/\/neuropediatoolbox.org\/?p=3693"},"modified":"2022-11-05T18:33:36","modified_gmt":"2022-11-05T18:33:36","slug":"sinaptopatias","status":"publish","type":"post","link":"https:\/\/neuropediatoolkit.org\/de\/sinaptopatias\/","title":{"rendered":"Synaptopathien."},"content":{"rendered":"<p>Beispiele f\u00fcr Synaptopathien von klinischem Interesse in der p\u00e4diatrischen Neurologie: <\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><em><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK396561\/\">STXBP1<\/a><\/em>. Es verursacht epileptische und fr\u00fche Entwicklungsenzephalopathie Typ 4. <\/li>\n\n\n\n<li><em><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK475803\/\">PRRT2<\/a><\/em>. Es f\u00fchrt unter anderem zu PRRT2-bedingten paroxysmalen Dyskinesien. <\/li>\n\n\n\n<li><em><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK274566\/\">TBC1D24<\/a><\/em>. Es f\u00fchrt zu epileptischer und entwicklungsbedingter Enzephalopathie Typ 16 sowie zu anderen Ph\u00e4notypen, wie z. B. progressiver myoklonischer Epilepsie. <\/li>\n\n\n\n<li><em><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1198\/\">SCHAFT3<\/a><\/em>. Es verursacht das Phelan-McDermid-Syndrom. <\/li>\n<\/ul>\n\n\n\n<p>Es gibt eine spanische Forschungsgruppe, die sich diesem Thema widmet <a href=\"http:\/\/www.connectingthegrowingbrain.com\/es\/\">Synaptopathien im Zusammenhang mit neurologischen Entwicklungsst\u00f6rungen<\/a>. <\/p>\n\n\n\n<p><\/p>","protected":false},"excerpt":{"rendered":"<p>Beispiele f\u00fcr Synaptopathien von klinischem Interesse in der p\u00e4diatrischen Neurologie: Es gibt eine spanische Forschungsgruppe, die sich Synaptopathien im Zusammenhang mit neurologischen Entwicklungsst\u00f6rungen widmet.<\/p>","protected":false},"author":1,"featured_media":3695,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_themeisle_gutenberg_block_has_review":false,"footnotes":""},"categories":[3,10,43],"tags":[],"class_list":["post-3693","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-enfermedades-neurologicas","category-neurogenetica","category-trastornos-del-neurodesarrollo","entry"],"_links":{"self":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/posts\/3693","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/comments?post=3693"}],"version-history":[{"count":0,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/posts\/3693\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/media\/3695"}],"wp:attachment":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/media?parent=3693"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/categories?post=3693"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/tags?post=3693"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}