{"id":108673,"date":"2021-05-26T11:13:51","date_gmt":"2021-05-26T11:13:51","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=108673"},"modified":"2023-07-30T06:18:20","modified_gmt":"2023-07-30T06:18:20","slug":"freeman-sheldon-syndrome","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/freeman-sheldon-syndrome\/","title":{"rendered":"Freeman-Sheldon syndrome"},"content":{"rendered":"<p>Freeman-Sheldon syndrome, also known as craniocarpotarsal dysplasia or whistling face syndrome, is a hereditary disorder with autosomal dominant transmission. The disorder manifests at birth and is characterized with a masklike \u201cwhistling\u201d face, hypoplastic alae nasi, ulnar deviation of the hands, flexion contractures of the fingers, and clubfeet.<\/p>\n<hr \/>\n<div class=\"group w-full text-gray-800 dark:text-gray-100 border-b border-black\/10 dark:border-gray-900\/50 bg-gray-50 dark:bg-[#444654] sm:AIPRM__conversation__response\">\n<div class=\"flex p-4 gap-4 text-base md:gap-6 md:max-w-2xl lg:max-w-[38rem] xl:max-w-3xl md:py-6 lg:px-0 m-auto\">\n<div class=\"relative flex w-[calc(100%-50px)] flex-col gap-1 md:gap-3 lg:w-[calc(100%-115px)]\">\n<div class=\"flex flex-grow flex-col gap-3\">\n<div class=\"min-h-[20px] flex items-start overflow-x-auto whitespace-pre-wrap break-words flex-col gap-4\">\n<div class=\"markdown prose w-full break-words dark:prose-invert light AIPRM__conversation__response\">\n<p>Freeman-Sheldon syndrome is an uncommon congenital disorder characterized by specific features, including sunken eyes, underdeveloped cartilage of the nose, pursed lips, various skeletal abnormalities, and muscle weakness. However, intelligence and life expectancy remain unaffected. This syndrome is typically inherited as an autosomal dominant genetic trait. Children affected by this condition may require corrective surgeries to address facial, hand, or foot deformities and improve their overall appearance and function.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Freeman-Sheldon syndrome, also known as craniocarpotarsal dysplasia or whistling face syndrome, is a hereditary disorder with autosomal dominant transmission. The disorder manifests at birth and is characterized with a masklike \u201cwhistling\u201d face, hypoplastic alae nasi, ulnar deviation of the hands, flexion contractures of the fingers, and clubfeet. Freeman-Sheldon syndrome is an uncommon congenital disorder characterized [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[6],"tags":[],"class_list":["post-108673","post","type-post","status-publish","format-standard","hentry","category-f"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Freeman-Sheldon syndrome - Definition of Freeman-Sheldon syndrome<\/title>\n<meta name=\"description\" content=\"Freeman-Sheldon syndrome, also known as craniocarpotarsal dysplasia or whistling face syndrome, is a hereditary disorder with autosomal dominant transmission. The disorder manifests at birth and is characterized with a masklike \u201cwhistling\u201d face, hypoplastic alae nasi, ulnar deviation of the hands, flexion contractures of the fingers, and clubfeet.Freeman-Sheldon syndrome is an uncommon congenital disorder characterized by specific features, including sunken eyes, underdeveloped cartilage of the nose, pursed lips, various skeletal abnormalities, and muscle weakness. However, intelligence and life expectancy remain unaffected. This syndrome is typically inherited as an autosomal dominant genetic trait. Children affected by this condition may require corrective surgeries to address facial, hand, or foot deformities and improve their overall appearance and function.\" \/>\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\/freeman-sheldon-syndrome\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Freeman-Sheldon syndrome - Definition of Freeman-Sheldon syndrome\" \/>\n<meta property=\"og:description\" content=\"Freeman-Sheldon syndrome, also known as craniocarpotarsal dysplasia or whistling face syndrome, is a hereditary disorder with autosomal dominant transmission. The disorder manifests at birth and is characterized with a masklike \u201cwhistling\u201d face, hypoplastic alae nasi, ulnar deviation of the hands, flexion contractures of the fingers, and clubfeet.Freeman-Sheldon syndrome is an uncommon congenital disorder characterized by specific features, including sunken eyes, underdeveloped cartilage of the nose, pursed lips, various skeletal abnormalities, and muscle weakness. However, intelligence and life expectancy remain unaffected. This syndrome is typically inherited as an autosomal dominant genetic trait. Children affected by this condition may require corrective surgeries to address facial, hand, or foot deformities and improve their overall appearance and function.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/freeman-sheldon-syndrome\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2021-05-26T11:13:51+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2023-07-30T06:18:20+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\/freeman-sheldon-syndrome\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/freeman-sheldon-syndrome\/\",\"name\":\"Freeman-Sheldon syndrome - Definition of Freeman-Sheldon syndrome\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2021-05-26T11:13:51+00:00\",\"dateModified\":\"2023-07-30T06:18:20+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"Freeman-Sheldon syndrome, also known as craniocarpotarsal dysplasia or whistling face syndrome, is a hereditary disorder with autosomal dominant transmission. The disorder manifests at birth and is characterized with a masklike \u201cwhistling\u201d face, hypoplastic alae nasi, ulnar deviation of the hands, flexion contractures of the fingers, and clubfeet.Freeman-Sheldon syndrome is an uncommon congenital disorder characterized by specific features, including sunken eyes, underdeveloped cartilage of the nose, pursed lips, various skeletal abnormalities, and muscle weakness. However, intelligence and life expectancy remain unaffected. This syndrome is typically inherited as an autosomal dominant genetic trait. 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