{"id":559,"date":"2013-06-29T03:01:44","date_gmt":"2013-06-29T03:01:44","guid":{"rendered":"https:\/\/blogs.bmj.com\/jmg\/?p=559"},"modified":"2026-02-25T20:06:20","modified_gmt":"2026-02-25T20:06:20","slug":"can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis","status":"publish","type":"post","link":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/","title":{"rendered":"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright)"},"content":{"rendered":"<p>The diagnosis of neurofibromatosis type I (NF1) has traditionally rested upon the presence of certain clinical features, including caf\u00e9-au-lait macules and freckling on the skin, and a variety of tumours, particularly neurofibromas. Skin changes are often the earliest manifestation, and therefore of particular significance when assessing people at risk of NF1. A rare, atypical, form of NF1 with few skin features and a predominance of spinal neurofibromas is known. Five affected families, in whom skin features were absent or very mild, were identified. Many affected individuals had severe pain and poor mobility from spinal tumours. Because of the lack of skin features, their diagnosis was often delayed, emphasising the importance of genetic testing for this condition. (<a href=\"http:\/\/jmg.bmj.com\/content\/early\/2013\/06\/27\/jmedgenet-2013-101648\">http:\/\/jmg.bmj.com\/content\/early\/2013\/06\/27\/jmedgenet-2013-101648<\/a> )<!--TrendMD v2.4.8--><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The diagnosis of neurofibromatosis type I (NF1) has traditionally rested upon the presence of certain clinical features, including caf\u00e9-au-lait macules and freckling on the skin, and a variety of tumours, particularly neurofibromas. Skin changes are often the earliest manifestation, and therefore of particular significance when assessing people at risk of NF1. A rare, atypical, form [&#8230;]<\/p>\n<p><a class=\"btn btn-secondary understrap-read-more-link\" href=\"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/\">Read More&#8230;<\/a><\/p>\n","protected":false},"author":123,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-559","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright) - JMG Contact blog<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright) - JMG Contact blog\" \/>\n<meta property=\"og:description\" content=\"The diagnosis of neurofibromatosis type I (NF1) has traditionally rested upon the presence of certain clinical features, including caf\u00e9-au-lait macules and freckling on the skin, and a variety of tumours, particularly neurofibromas. Skin changes are often the earliest manifestation, and therefore of particular significance when assessing people at risk of NF1. A rare, atypical, form [...]Read More...\" \/>\n<meta property=\"og:url\" content=\"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/\" \/>\n<meta property=\"og:site_name\" content=\"JMG Contact blog\" \/>\n<meta property=\"article:published_time\" content=\"2013-06-29T03:01:44+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2026-02-25T20:06:20+00:00\" \/>\n<meta name=\"author\" content=\"hqqu\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@HuiQiQu\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"hqqu\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/\"},\"author\":{\"name\":\"hqqu\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#\\\/schema\\\/person\\\/be0250f8d5b52412c3e7c222dabd591b\"},\"headline\":\"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright)\",\"datePublished\":\"2013-06-29T03:01:44+00:00\",\"dateModified\":\"2026-02-25T20:06:20+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/\"},\"wordCount\":156,\"commentCount\":0,\"publisher\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#organization\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"CommentAction\",\"name\":\"Comment\",\"target\":[\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/#respond\"]}]},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/\",\"url\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/\",\"name\":\"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright) - JMG Contact blog\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#website\"},\"datePublished\":\"2013-06-29T03:01:44+00:00\",\"dateModified\":\"2026-02-25T20:06:20+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2013\\\/06\\\/29\\\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright)\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#website\",\"url\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/\",\"name\":\"JMG Contact blog\",\"description\":\"JMG Contact blog\",\"publisher\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#organization\",\"name\":\"JMG Contact blog\",\"url\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/files\\\/2017\\\/10\\\/blog-logo-jmg.png\",\"contentUrl\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/files\\\/2017\\\/10\\\/blog-logo-jmg.png\",\"width\":300,\"height\":34,\"caption\":\"JMG Contact blog\"},\"image\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#\\\/schema\\\/logo\\\/image\\\/\"}},{\"@type\":\"Person\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#\\\/schema\\\/person\\\/be0250f8d5b52412c3e7c222dabd591b\",\"name\":\"hqqu\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/920bc4e81500cde88def4bfd7775029cb154e422c5460b9cf80d5c47137d6f35?s=96&d=mm&r=g\",\"url\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/920bc4e81500cde88def4bfd7775029cb154e422c5460b9cf80d5c47137d6f35?s=96&d=mm&r=g\",\"contentUrl\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/920bc4e81500cde88def4bfd7775029cb154e422c5460b9cf80d5c47137d6f35?s=96&d=mm&r=g\",\"caption\":\"hqqu\"},\"description\":\"Huiqi Qu has a background as a physician trained in internal medicine and a PhD in Experimental Medicine (Endocrinology). His research applies human genetics and multi-omics to complex and pediatric diseases, including GWAS, polygenic risk scores (PRS), single-cell transcriptomics, and integrative genomics to support precision medicine and clinical translation.\",\"sameAs\":[\"https:\\\/\\\/x.com\\\/HuiQiQu\"],\"url\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/author\\\/hqiqu\\\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright) - JMG Contact blog","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/","og_locale":"en_US","og_type":"article","og_title":"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright) - JMG Contact blog","og_description":"The diagnosis of neurofibromatosis type I (NF1) has traditionally rested upon the presence of certain clinical features, including caf\u00e9-au-lait macules and freckling on the skin, and a variety of tumours, particularly neurofibromas. Skin changes are often the earliest manifestation, and therefore of particular significance when assessing people at risk of NF1. A rare, atypical, form [...]Read More...","og_url":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/","og_site_name":"JMG Contact blog","article_published_time":"2013-06-29T03:01:44+00:00","article_modified_time":"2026-02-25T20:06:20+00:00","author":"hqqu","twitter_card":"summary_large_image","twitter_creator":"@HuiQiQu","twitter_misc":{"Written by":"hqqu","Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/#article","isPartOf":{"@id":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/"},"author":{"name":"hqqu","@id":"https:\/\/blogs.bmj.com\/jmg\/#\/schema\/person\/be0250f8d5b52412c3e7c222dabd591b"},"headline":"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright)","datePublished":"2013-06-29T03:01:44+00:00","dateModified":"2026-02-25T20:06:20+00:00","mainEntityOfPage":{"@id":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/"},"wordCount":156,"commentCount":0,"publisher":{"@id":"https:\/\/blogs.bmj.com\/jmg\/#organization"},"inLanguage":"en-US","potentialAction":[{"@type":"CommentAction","name":"Comment","target":["https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/#respond"]}]},{"@type":"WebPage","@id":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/","url":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/","name":"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright) - JMG Contact blog","isPartOf":{"@id":"https:\/\/blogs.bmj.com\/jmg\/#website"},"datePublished":"2013-06-29T03:01:44+00:00","dateModified":"2026-02-25T20:06:20+00:00","breadcrumb":{"@id":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/blogs.bmj.com\/jmg\/2013\/06\/29\/can-the-diagnosis-of-nf1-be-excluded-clinically-a-lack-of-pigmentary-findings-in-families-with-spinal-neurofibromatosis-demonstrates-a-limitation-of-clinical-diagnosis\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/blogs.bmj.com\/jmg\/"},{"@type":"ListItem","position":2,"name":"Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright)"}]},{"@type":"WebSite","@id":"https:\/\/blogs.bmj.com\/jmg\/#website","url":"https:\/\/blogs.bmj.com\/jmg\/","name":"JMG Contact blog","description":"JMG Contact blog","publisher":{"@id":"https:\/\/blogs.bmj.com\/jmg\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/blogs.bmj.com\/jmg\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/blogs.bmj.com\/jmg\/#organization","name":"JMG Contact blog","url":"https:\/\/blogs.bmj.com\/jmg\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/blogs.bmj.com\/jmg\/#\/schema\/logo\/image\/","url":"https:\/\/blogs.bmj.com\/jmg\/files\/2017\/10\/blog-logo-jmg.png","contentUrl":"https:\/\/blogs.bmj.com\/jmg\/files\/2017\/10\/blog-logo-jmg.png","width":300,"height":34,"caption":"JMG Contact blog"},"image":{"@id":"https:\/\/blogs.bmj.com\/jmg\/#\/schema\/logo\/image\/"}},{"@type":"Person","@id":"https:\/\/blogs.bmj.com\/jmg\/#\/schema\/person\/be0250f8d5b52412c3e7c222dabd591b","name":"hqqu","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/secure.gravatar.com\/avatar\/920bc4e81500cde88def4bfd7775029cb154e422c5460b9cf80d5c47137d6f35?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/920bc4e81500cde88def4bfd7775029cb154e422c5460b9cf80d5c47137d6f35?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/920bc4e81500cde88def4bfd7775029cb154e422c5460b9cf80d5c47137d6f35?s=96&d=mm&r=g","caption":"hqqu"},"description":"Huiqi Qu has a background as a physician trained in internal medicine and a PhD in Experimental Medicine (Endocrinology). His research applies human genetics and multi-omics to complex and pediatric diseases, including GWAS, polygenic risk scores (PRS), single-cell transcriptomics, and integrative genomics to support precision medicine and clinical translation.","sameAs":["https:\/\/x.com\/HuiQiQu"],"url":"https:\/\/blogs.bmj.com\/jmg\/author\/hqiqu\/"}]}},"_links":{"self":[{"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/posts\/559","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/users\/123"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/comments?post=559"}],"version-history":[{"count":0,"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/posts\/559\/revisions"}],"wp:attachment":[{"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/media?parent=559"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/categories?post=559"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.bmj.com\/jmg\/wp-json\/wp\/v2\/tags?post=559"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}