{"id":108807,"date":"2021-05-27T08:17:16","date_gmt":"2021-05-27T08:17:16","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=108807"},"modified":"2023-07-21T07:59:07","modified_gmt":"2023-07-21T07:59:07","slug":"chanarin-dorfman-syndrome","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/","title":{"rendered":"Chanarin dorfman syndrome"},"content":{"rendered":"<p>Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome.<\/p>\n<hr \/>\n<p>This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. The disorder is present from birth and is known for causing ichthyosis, which manifests as thickened, scaly skin. Additionally, it leads to myopathy, a muscle degeneration, and in some cases, it may also result in visual and auditory defects. Blood tests reveal atypical white blood cells that contain tiny spaces filled with fat.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome. This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[3],"tags":[],"class_list":["post-108807","post","type-post","status-publish","format-standard","hentry","category-c"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Chanarin dorfman syndrome - Definition of Chanarin dorfman syndrome<\/title>\n<meta name=\"description\" content=\"Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome.This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. The disorder is present from birth and is known for causing ichthyosis, which manifests as thickened, scaly skin. Additionally, it leads to myopathy, a muscle degeneration, and in some cases, it may also result in visual and auditory defects. Blood tests reveal atypical white blood cells that contain tiny spaces filled with fat.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Chanarin dorfman syndrome - Definition of Chanarin dorfman syndrome\" \/>\n<meta property=\"og:description\" content=\"Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome.This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. The disorder is present from birth and is known for causing ichthyosis, which manifests as thickened, scaly skin. Additionally, it leads to myopathy, a muscle degeneration, and in some cases, it may also result in visual and auditory defects. Blood tests reveal atypical white blood cells that contain tiny spaces filled with fat.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2021-05-27T08:17:16+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2023-07-21T07:59:07+00:00\" \/>\n<meta name=\"author\" content=\"Glossary\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Glossary\" \/>\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\":\"WebPage\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/\",\"name\":\"Chanarin dorfman syndrome - Definition of Chanarin dorfman syndrome\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2021-05-27T08:17:16+00:00\",\"dateModified\":\"2023-07-21T07:59:07+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome.This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. The disorder is present from birth and is known for causing ichthyosis, which manifests as thickened, scaly skin. Additionally, it leads to myopathy, a muscle degeneration, and in some cases, it may also result in visual and auditory defects. Blood tests reveal atypical white blood cells that contain tiny spaces filled with fat.\",\"breadcrumb\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Chanarin dorfman syndrome\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/\",\"name\":\"Glossary\",\"description\":\"Difinitions\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\",\"name\":\"Glossary\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/author\/adminglossary\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Chanarin dorfman syndrome - Definition of Chanarin dorfman syndrome","description":"Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome.This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. The disorder is present from birth and is known for causing ichthyosis, which manifests as thickened, scaly skin. Additionally, it leads to myopathy, a muscle degeneration, and in some cases, it may also result in visual and auditory defects. Blood tests reveal atypical white blood cells that contain tiny spaces filled with fat.","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:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/","og_locale":"en_US","og_type":"article","og_title":"Chanarin dorfman syndrome - Definition of Chanarin dorfman syndrome","og_description":"Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome.This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. The disorder is present from birth and is known for causing ichthyosis, which manifests as thickened, scaly skin. Additionally, it leads to myopathy, a muscle degeneration, and in some cases, it may also result in visual and auditory defects. Blood tests reveal atypical white blood cells that contain tiny spaces filled with fat.","og_url":"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/","og_site_name":"Glossary","article_published_time":"2021-05-27T08:17:16+00:00","article_modified_time":"2023-07-21T07:59:07+00:00","author":"Glossary","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Glossary","Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/","name":"Chanarin dorfman syndrome - Definition of Chanarin dorfman syndrome","isPartOf":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#website"},"datePublished":"2021-05-27T08:17:16+00:00","dateModified":"2023-07-21T07:59:07+00:00","author":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5"},"description":"Chanarin Dorfman syndrome is a hereditary disorder of lipid metabolism almost always accompanied by dry, scaly skin (ichthyosis). Myopathy (degeneration of the muscles) and fat deposits appearing in the white blood cells also are commonly seen in patients with Chanarin Dorfman syndrome.This is a highly uncommon autosomal recessive genetic condition that impacts fat metabolism. The disorder is present from birth and is known for causing ichthyosis, which manifests as thickened, scaly skin. Additionally, it leads to myopathy, a muscle degeneration, and in some cases, it may also result in visual and auditory defects. Blood tests reveal atypical white blood cells that contain tiny spaces filled with fat.","breadcrumb":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/chanarin-dorfman-syndrome\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.healthbenefitstimes.com\/glossary\/"},{"@type":"ListItem","position":2,"name":"Chanarin dorfman syndrome"}]},{"@type":"WebSite","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#website","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/","name":"Glossary","description":"Difinitions","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.healthbenefitstimes.com\/glossary\/?s={search_term_string}"},"query-input":"required name=search_term_string"}],"inLanguage":"en-US"},{"@type":"Person","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5","name":"Glossary","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/author\/adminglossary\/"}]}},"_links":{"self":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/108807","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/comments?post=108807"}],"version-history":[{"count":3,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/108807\/revisions"}],"predecessor-version":[{"id":234253,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/108807\/revisions\/234253"}],"wp:attachment":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/media?parent=108807"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/categories?post=108807"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/tags?post=108807"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}