{"id":109160,"date":"2021-05-30T11:09:40","date_gmt":"2021-05-30T11:09:40","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=109160"},"modified":"2021-05-30T11:09:40","modified_gmt":"2021-05-30T11:09:40","slug":"peters-plus-syndrome","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/peters-plus-syndrome\/","title":{"rendered":"Peters plus syndrome"},"content":{"rendered":"<p>Peters\u2019-plus syndrome, also known as Peter s syndrome, is widely believed to be an autosomal recessively inherited disorder and thus occurs infrequently. Currently there appears to be some consensus that Peters -plus syndrome and Krause-Kivlin Syndrome (or Kivlin syndrome) are the same disorder. Peters\u2019-Plus Syndrome is characterized by a typical face, short limb dwarfism, Peter\u2019s anomaly (a corneal abnormality), and growth retardation. In many cases, cleft lip and palate, visceral anomalies, and mental retardation are also present. Increased incidence of fetal loss in families in which Peters\u2019-plus syndrome is present suggests the intrauterine death of some fetuses affected by Peters\u2019-plus syndrome.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Peters\u2019-plus syndrome, also known as Peter s syndrome, is widely believed to be an autosomal recessively inherited disorder and thus occurs infrequently. Currently there appears to be some consensus that Peters -plus syndrome and Krause-Kivlin Syndrome (or Kivlin syndrome) are the same disorder. Peters\u2019-Plus Syndrome is characterized by a typical face, short limb dwarfism, Peter\u2019s [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[16],"tags":[],"class_list":["post-109160","post","type-post","status-publish","format-standard","hentry","category-p"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Peters plus syndrome - Definition of Peters plus syndrome<\/title>\n<meta name=\"description\" content=\"Peters\u2019-plus syndrome, also known as Peter s syndrome, is widely believed to be an autosomal recessively inherited disorder and thus occurs infrequently. Currently there appears to be some consensus that Peters -plus syndrome and Krause-Kivlin Syndrome (or Kivlin syndrome) are the same disorder. Peters\u2019-Plus Syndrome is characterized by a typical face, short limb dwarfism, Peter\u2019s anomaly (a corneal abnormality), and growth retardation. In many cases, cleft lip and palate, visceral anomalies, and mental retardation are also present. Increased incidence of fetal loss in families in which Peters\u2019-plus syndrome is present suggests the intrauterine death of some fetuses affected by Peters\u2019-plus syndrome.\" \/>\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\/peters-plus-syndrome\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Peters plus syndrome - Definition of Peters plus syndrome\" \/>\n<meta property=\"og:description\" content=\"Peters\u2019-plus syndrome, also known as Peter s syndrome, is widely believed to be an autosomal recessively inherited disorder and thus occurs infrequently. Currently there appears to be some consensus that Peters -plus syndrome and Krause-Kivlin Syndrome (or Kivlin syndrome) are the same disorder. Peters\u2019-Plus Syndrome is characterized by a typical face, short limb dwarfism, Peter\u2019s anomaly (a corneal abnormality), and growth retardation. In many cases, cleft lip and palate, visceral anomalies, and mental retardation are also present. Increased incidence of fetal loss in families in which Peters\u2019-plus syndrome is present suggests the intrauterine death of some fetuses affected by Peters\u2019-plus syndrome.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/peters-plus-syndrome\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2021-05-30T11:09:40+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\/peters-plus-syndrome\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/peters-plus-syndrome\/\",\"name\":\"Peters plus syndrome - Definition of Peters plus syndrome\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2021-05-30T11:09:40+00:00\",\"dateModified\":\"2021-05-30T11:09:40+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"Peters\u2019-plus syndrome, also known as Peter s syndrome, is widely believed to be an autosomal recessively inherited disorder and thus occurs infrequently. Currently there appears to be some consensus that Peters -plus syndrome and Krause-Kivlin Syndrome (or Kivlin syndrome) are the same disorder. Peters\u2019-Plus Syndrome is characterized by a typical face, short limb dwarfism, Peter\u2019s anomaly (a corneal abnormality), and growth retardation. In many cases, cleft lip and palate, visceral anomalies, and mental retardation are also present. 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