{"id":236757,"date":"2023-08-11T06:44:45","date_gmt":"2023-08-11T06:44:45","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=236757"},"modified":"2023-08-11T06:44:45","modified_gmt":"2023-08-11T06:44:45","slug":"maroteaux-lamy-syndrome","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/maroteaux-lamy-syndrome\/","title":{"rendered":"Maroteaux\u2013Lamy syndrome"},"content":{"rendered":"<div class=\"group w-full text-token-text-primary border-b border-black\/10 dark:border-gray-900\/50 bg-gray-50 dark:bg-[#444654]\">\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 flex-col items-start gap-3 overflow-x-auto whitespace-pre-wrap break-words\">\n<div class=\"markdown prose w-full break-words dark:prose-invert light AIPRM__conversation__response\">\n<p>A type of mucopolysaccharidosis arises due to insufficient levels of the enzyme arylsulfatase B. This leads to symptoms akin to those observed in Hurler&#8217;s syndrome, including facial feature coarsening, skeletal distortions, cardiac irregularities, and enlargement of the liver and spleen. However, in this form, the child&#8217;s intelligence level remains normal. Typically emerging during early childhood, the condition lacks a distinct treatment, and heart failure-related mortality often transpires between the ages of 20 and 30.<\/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>A type of mucopolysaccharidosis arises due to insufficient levels of the enzyme arylsulfatase B. This leads to symptoms akin to those observed in Hurler&#8217;s syndrome, including facial feature coarsening, skeletal distortions, cardiac irregularities, and enlargement of the liver and spleen. However, in this form, the child&#8217;s intelligence level remains normal. Typically emerging during early childhood, [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":["post-236757","post","type-post","status-publish","format-standard","hentry","category-m"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Maroteaux\u2013Lamy syndrome - Definition of Maroteaux\u2013Lamy syndrome<\/title>\n<meta name=\"description\" content=\"A type of mucopolysaccharidosis arises due to insufficient levels of the enzyme arylsulfatase B. This leads to symptoms akin to those observed in Hurler&#039;s syndrome, including facial feature coarsening, skeletal distortions, cardiac irregularities, and enlargement of the liver and spleen. However, in this form, the child&#039;s intelligence level remains normal. Typically emerging during early childhood, the condition lacks a distinct treatment, and heart failure-related mortality often transpires between the ages of 20 and 30.\" \/>\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\/maroteaux-lamy-syndrome\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Maroteaux\u2013Lamy syndrome - Definition of Maroteaux\u2013Lamy syndrome\" \/>\n<meta property=\"og:description\" content=\"A type of mucopolysaccharidosis arises due to insufficient levels of the enzyme arylsulfatase B. This leads to symptoms akin to those observed in Hurler&#039;s syndrome, including facial feature coarsening, skeletal distortions, cardiac irregularities, and enlargement of the liver and spleen. 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