{"id":33675,"date":"2022-07-11T17:56:47","date_gmt":"2022-07-11T08:56:47","guid":{"rendered":"https:\/\/www.hiro-clinic.or.jp\/nipt\/?page_id=33675"},"modified":"2024-01-05T17:18:54","modified_gmt":"2024-01-05T08:18:54","slug":"pontocerebellar-hypoplasia-type-2d","status":"publish","type":"genetic-diseases","link":"https:\/\/www.hiro-clinic.or.jp\/nipt\/genetic-diseases2\/pontocerebellar-hypoplasia-type-2d\/","title":{"rendered":"\u6a4b\u5c0f\u8133\u5f62\u6210\u4e0d\u51682D\u578b"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\">\u6982\u8981<\/h2>\n\n\n\n<p>\u9032\u884c\u6027\u5927\u8133\u8133\u840e\u7e2e\u75c7\uff08PCCA\uff09\u3068\u3057\u3066\u3082\u77e5\u3089\u308c\u308b\u6a4b\u5c0f\u8133\u5f62\u6210\u4e0d\u51682D\u578b\uff08PCH2D\uff09\u306f\u3001PCH2D\u306f\u3001\u9032\u884c\u6027\u5c0f\u982d\u75c7\u3001\u5927\u8133\u304a\u3088\u3073\u5c0f\u8133\u306e\u9032\u884c\u6027\u840e\u7e2e\u306e\u51fa\u751f\u5f8c\u767a\u75c7\u3001\u91cd\u5ea6\u306e\u7cbe\u795e\u9045\u6ede\u3001\u75d9\u7e2e\u3001\u304a\u3088\u3073\u3055\u307e\u3056\u307e\u306a\u767a\u4f5c\u3092\u7279\u5fb4\u3068\u3059\u308b\u5e38\u67d3\u8272\u4f53\u52a3\u6027\u75be\u60a3\u3067\u3059\u3002<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">\u75ab\u5b66<\/h2>\n\n\n\n<p>\u4e00\u822c\u7684\u306a\u5c0f\u5150\u96c6\u56e3\u5185\u30671\uff1a200.000\u672a\u6e80\u3068\u8a08\u7b97\u3055\u308c\u3066\u3044\u307e\u3059\u3002<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">\u539f\u56e0<\/h2>\n\n\n\n<p>\u67d3\u8272\u4f534p15\u306eSEPSECS\u907a\u4f1d\u5b50\uff08613009\uff09\u306e\u30db\u30e2\u63a5\u5408\u307e\u305f\u306f\u8907\u5408\u30d8\u30c6\u30ed\u63a5\u5408\u5909\u7570\u306b\u3088\u3063\u3066\u5f15\u304d\u8d77\u3053\u3055\u308c\u307e\u3059\u3002<\/p>\n\n\nSEPSECS\u907a\u4f1d\u5b50\u3067\u3042\u308c\u3070\u5f53\u9662\u306e<a href=\"https:\/\/www.hiro-clinic.or.jp\/nipt\/plan\/n-advance\/\">N-advance FM+\u30d7\u30e9\u30f3<\/a>\u30fb<a href=\"https:\/\/www.hiro-clinic.or.jp\/nipt\/plan\/n-advance\/\">N-advance GM+\u30d7\u30e9\u30f3<\/a>\u3067\u691c\u67fb\u304c\u53ef\u80fd\u3068\u306a\u3063\u3066\u304a\u308a\u307e\u3059\u3002\n\n\n<h2 class=\"wp-block-heading\">\u75c7\u72b6<\/h2>\n\n\n\n<p>\u4e3b\u306a\u81e8\u5e8a\u7684\u7279\u5fb4\u306f\u3001\u91cd\u5ea6\u306e\u7cbe\u795e\u904b\u52d5\u9045\u5ef6\u3068\u5c0f\u982d\u75c7\u3092\u7279\u5fb4\u3068\u3057\u3066\u3044\u307e\u3059\u3002<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">\u8a3a\u65ad<\/h2>\n\n\n\n<p>\u5c0f\u982d\u75c7\u306f\u901a\u5e38\u3001\u51fa\u751f\u6642\u306b\u306f\u660e\u3089\u304b\u3067\u306f\u3042\u308a\u307e\u305b\u3093\u304c\u3001\u4e73\u5150\u671f\u3068\u5e7c\u5150\u671f\u306b\u8133\u306e\u6210\u9577\u304c\u9045\u3044\u307e\u307e\u3067\u3042\u308b\u305f\u3081\u3001\u9855\u8457\u306b\u306a\u308a\u307e\u3059\u3002<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">\u4e88\u5f8c<\/h2>\n\n\n\n<p>PCH\u306f\u4e88\u5f8c\u304c\u60aa\u304f\u3001\u5e7c\u5150\u671f\u306b\u306f\u81f4\u547d\u7684\u3067\u3059\u3002<\/p>\n\n\n\n<div class=\"wp-block-group references\"><div class=\"wp-block-group__inner-container is-layout-flow wp-block-group-is-layout-flow\">\n<p>\u3010\u53c2\u8003\u6587\u732e\u3011<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>OMIM &#8211; <a href=\"https:\/\/www.omim.org\/entry\/613811\" data-type=\"URL\" data-id=\"https:\/\/www.omim.org\/entry\/613811\">PONTOCEREBELLAR HYPOPLASIA, TYPE 2D; PCH2D<\/a><\/li>\n\n\n\n<li>NIH &#8211; <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/medgen\/462490\" data-type=\"URL\" data-id=\"https:\/\/www.ncbi.nlm.nih.gov\/medgen\/462490\">Pontocerebellar hypoplasia type 2D(PCH2D)<\/a><\/li>\n\n\n\n<li>ScienceDirect &#8211; <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S1090379816000052\" data-type=\"URL\" data-id=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S1090379816000052\">Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency<\/a><\/li>\n<\/ul>\n<\/div><\/div>\n","protected":false},"featured_media":0,"menu_order":31,"template":"page_gd.php","class_list":["post-33675","genetic-diseases","type-genetic-diseases","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.hiro-clinic.or.jp\/nipt\/wp-json\/wp\/v2\/genetic-diseases\/33675","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.hiro-clinic.or.jp\/nipt\/wp-json\/wp\/v2\/genetic-diseases"}],"about":[{"href":"https:\/\/www.hiro-clinic.or.jp\/nipt\/wp-json\/wp\/v2\/types\/genetic-diseases"}],"version-history":[{"count":4,"href":"https:\/\/www.hiro-clinic.or.jp\/nipt\/wp-json\/wp\/v2\/genetic-diseases\/33675\/revisions"}],"predecessor-version":[{"id":70424,"href":"https:\/\/www.hiro-clinic.or.jp\/nipt\/wp-json\/wp\/v2\/genetic-diseases\/33675\/revisions\/70424"}],"wp:attachment":[{"href":"https:\/\/www.hiro-clinic.or.jp\/nipt\/wp-json\/wp\/v2\/media?parent=33675"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}