{"id":25857,"date":"2020-07-03T08:30:09","date_gmt":"2020-07-03T08:30:09","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=25857"},"modified":"2022-04-19T04:54:07","modified_gmt":"2022-04-19T04:54:07","slug":"angelmans-syndrome","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/","title":{"rendered":"Angelman\u2019s syndrome"},"content":{"rendered":"<p>A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15.<\/p>\n<hr \/>\n<p>Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and appearance of a marionette, is a rare congenital neurodevelopmental disorder with complex genetic etiology. It is manifested by mental retardation, speech impairment, movement disorder, and easily- provoked laughter. Dysmorphic facial features frequently occur. The condition was first reported by the English pediatrician, Harry Angelman. The condition is usually not recognized at birth or in infancy due to nonspecific features. Average age of diagnosis is 6 years.<\/p>\n<hr \/>\n<p>A rare genetic condition marked by severe mental retardation, microcephaly, and paroxysms of laughter. It is due to an abnormal chromosome 15 of maternal origin.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15. Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-25857","post","type-post","status-publish","format-standard","hentry","category-a"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Angelman\u2019s syndrome - Definition of Angelman\u2019s syndrome<\/title>\n<meta name=\"description\" content=\"A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15.Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and appearance of a marionette, is a rare congenital neurodevelopmental disorder with complex genetic etiology. It is manifested by mental retardation, speech impairment, movement disorder, and easily- provoked laughter. Dysmorphic facial features frequently occur. The condition was first reported by the English pediatrician, Harry Angelman. The condition is usually not recognized at birth or in infancy due to nonspecific features. Average age of diagnosis is 6 years.A rare genetic condition marked by severe mental retardation, microcephaly, and paroxysms of laughter. It is due to an abnormal chromosome 15 of maternal origin.\" \/>\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\/angelmans-syndrome\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Angelman\u2019s syndrome - Definition of Angelman\u2019s syndrome\" \/>\n<meta property=\"og:description\" content=\"A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15.Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and appearance of a marionette, is a rare congenital neurodevelopmental disorder with complex genetic etiology. It is manifested by mental retardation, speech impairment, movement disorder, and easily- provoked laughter. Dysmorphic facial features frequently occur. The condition was first reported by the English pediatrician, Harry Angelman. The condition is usually not recognized at birth or in infancy due to nonspecific features. Average age of diagnosis is 6 years.A rare genetic condition marked by severe mental retardation, microcephaly, and paroxysms of laughter. It is due to an abnormal chromosome 15 of maternal origin.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2020-07-03T08:30:09+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2022-04-19T04:54:07+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\/angelmans-syndrome\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/\",\"name\":\"Angelman\u2019s syndrome - Definition of Angelman\u2019s syndrome\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2020-07-03T08:30:09+00:00\",\"dateModified\":\"2022-04-19T04:54:07+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15.Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and appearance of a marionette, is a rare congenital neurodevelopmental disorder with complex genetic etiology. It is manifested by mental retardation, speech impairment, movement disorder, and easily- provoked laughter. Dysmorphic facial features frequently occur. The condition was first reported by the English pediatrician, Harry Angelman. The condition is usually not recognized at birth or in infancy due to nonspecific features. Average age of diagnosis is 6 years.A rare genetic condition marked by severe mental retardation, microcephaly, and paroxysms of laughter. It is due to an abnormal chromosome 15 of maternal origin.\",\"breadcrumb\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Angelman\u2019s 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":"Angelman\u2019s syndrome - Definition of Angelman\u2019s syndrome","description":"A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15.Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and appearance of a marionette, is a rare congenital neurodevelopmental disorder with complex genetic etiology. It is manifested by mental retardation, speech impairment, movement disorder, and easily- provoked laughter. Dysmorphic facial features frequently occur. The condition was first reported by the English pediatrician, Harry Angelman. The condition is usually not recognized at birth or in infancy due to nonspecific features. Average age of diagnosis is 6 years.A rare genetic condition marked by severe mental retardation, microcephaly, and paroxysms of laughter. It is due to an abnormal chromosome 15 of maternal origin.","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\/angelmans-syndrome\/","og_locale":"en_US","og_type":"article","og_title":"Angelman\u2019s syndrome - Definition of Angelman\u2019s syndrome","og_description":"A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15.Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and appearance of a marionette, is a rare congenital neurodevelopmental disorder with complex genetic etiology. It is manifested by mental retardation, speech impairment, movement disorder, and easily- provoked laughter. Dysmorphic facial features frequently occur. The condition was first reported by the English pediatrician, Harry Angelman. The condition is usually not recognized at birth or in infancy due to nonspecific features. Average age of diagnosis is 6 years.A rare genetic condition marked by severe mental retardation, microcephaly, and paroxysms of laughter. It is due to an abnormal chromosome 15 of maternal origin.","og_url":"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/","og_site_name":"Glossary","article_published_time":"2020-07-03T08:30:09+00:00","article_modified_time":"2022-04-19T04:54:07+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\/angelmans-syndrome\/","url":"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/","name":"Angelman\u2019s syndrome - Definition of Angelman\u2019s syndrome","isPartOf":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#website"},"datePublished":"2020-07-03T08:30:09+00:00","dateModified":"2022-04-19T04:54:07+00:00","author":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5"},"description":"A genetic disorder characterized by intellectual and developmental delay, seizures, jerky movements, ataxia, hyperactivity, skin and eye hypopigmentation, and unprovoked laughter. The syndrome is caused by a deletion of a segment of chromosome 15.Angelman syndrome, formerly known as happy puppet syndrome due to a resemblance of children with the disorder to the movement and appearance of a marionette, is a rare congenital neurodevelopmental disorder with complex genetic etiology. It is manifested by mental retardation, speech impairment, movement disorder, and easily- provoked laughter. Dysmorphic facial features frequently occur. The condition was first reported by the English pediatrician, Harry Angelman. The condition is usually not recognized at birth or in infancy due to nonspecific features. Average age of diagnosis is 6 years.A rare genetic condition marked by severe mental retardation, microcephaly, and paroxysms of laughter. It is due to an abnormal chromosome 15 of maternal origin.","breadcrumb":{"@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.healthbenefitstimes.com\/glossary\/angelmans-syndrome\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.healthbenefitstimes.com\/glossary\/"},{"@type":"ListItem","position":2,"name":"Angelman\u2019s 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\/25857","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=25857"}],"version-history":[{"count":3,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/25857\/revisions"}],"predecessor-version":[{"id":153880,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/posts\/25857\/revisions\/153880"}],"wp:attachment":[{"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/media?parent=25857"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/categories?post=25857"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-json\/wp\/v2\/tags?post=25857"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}