{"id":109227,"date":"2021-05-31T06:21:41","date_gmt":"2021-05-31T06:21:41","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=109227"},"modified":"2021-05-31T06:21:41","modified_gmt":"2021-05-31T06:21:41","slug":"rapp-hodgkin-syndrome","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/rapp-hodgkin-syndrome\/","title":{"rendered":"Rapp-hodgkin syndrome"},"content":{"rendered":"<p>Rapp-Hodgkin syndrome (RHS) belongs to a group of genetic disorders known as ectodermal dysplasia syndromes. In general, ectodermal dysplasia syndromes are caused by defects in the formation of the ectoderm (the outermost layer of embryonic tissue) during gestation. Ectodermal dysplasia syndromes are multisystem disorders that are characterized by the deficient function or absence of at least two of the following ectodermal structures: skin, teeth, hair, nails, and glands (National Foundation for Ectodermal Dysplasias [NFED], 2001). More than 200 clinically or genetically distinct forms of ectodermal dysplasia have been identified, with classification based on the following considerations: extent, nature, and severity of ectodermal involvement; the presence of associated malformations; and the mode of inheritance.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Rapp-Hodgkin syndrome (RHS) belongs to a group of genetic disorders known as ectodermal dysplasia syndromes. In general, ectodermal dysplasia syndromes are caused by defects in the formation of the ectoderm (the outermost layer of embryonic tissue) during gestation. Ectodermal dysplasia syndromes are multisystem disorders that are characterized by the deficient function or absence of at [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[18],"tags":[],"class_list":["post-109227","post","type-post","status-publish","format-standard","hentry","category-r"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Rapp-hodgkin syndrome - Definition of Rapp-hodgkin syndrome<\/title>\n<meta name=\"description\" content=\"Rapp-Hodgkin syndrome (RHS) belongs to a group of genetic disorders known as ectodermal dysplasia syndromes. In general, ectodermal dysplasia syndromes are caused by defects in the formation of the ectoderm (the outermost layer of embryonic tissue) during gestation. Ectodermal dysplasia syndromes are multisystem disorders that are characterized by the deficient function or absence of at least two of the following ectodermal structures: skin, teeth, hair, nails, and glands (National Foundation for Ectodermal Dysplasias [NFED], 2001). More than 200 clinically or genetically distinct forms of ectodermal dysplasia have been identified, with classification based on the following considerations: extent, nature, and severity of ectodermal involvement; the presence of associated malformations; and the mode of inheritance.\" \/>\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\/rapp-hodgkin-syndrome\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Rapp-hodgkin syndrome - Definition of Rapp-hodgkin syndrome\" \/>\n<meta property=\"og:description\" content=\"Rapp-Hodgkin syndrome (RHS) belongs to a group of genetic disorders known as ectodermal dysplasia syndromes. In general, ectodermal dysplasia syndromes are caused by defects in the formation of the ectoderm (the outermost layer of embryonic tissue) during gestation. Ectodermal dysplasia syndromes are multisystem disorders that are characterized by the deficient function or absence of at least two of the following ectodermal structures: skin, teeth, hair, nails, and glands (National Foundation for Ectodermal Dysplasias [NFED], 2001). More than 200 clinically or genetically distinct forms of ectodermal dysplasia have been identified, with classification based on the following considerations: extent, nature, and severity of ectodermal involvement; the presence of associated malformations; and the mode of inheritance.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/rapp-hodgkin-syndrome\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2021-05-31T06:21:41+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\/rapp-hodgkin-syndrome\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/rapp-hodgkin-syndrome\/\",\"name\":\"Rapp-hodgkin syndrome - Definition of Rapp-hodgkin syndrome\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2021-05-31T06:21:41+00:00\",\"dateModified\":\"2021-05-31T06:21:41+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"Rapp-Hodgkin syndrome (RHS) belongs to a group of genetic disorders known as ectodermal dysplasia syndromes. In general, ectodermal dysplasia syndromes are caused by defects in the formation of the ectoderm (the outermost layer of embryonic tissue) during gestation. Ectodermal dysplasia syndromes are multisystem disorders that are characterized by the deficient function or absence of at least two of the following ectodermal structures: skin, teeth, hair, nails, and glands (National Foundation for Ectodermal Dysplasias [NFED], 2001). 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