{"id":182238,"date":"2022-09-12T10:00:32","date_gmt":"2022-09-12T10:00:32","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=182238"},"modified":"2023-08-11T04:39:19","modified_gmt":"2023-08-11T04:39:19","slug":"lysosomal-storage-disease","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/lysosomal-storage-disease\/","title":{"rendered":"Lysosomal storage disease"},"content":{"rendered":"<p>A disease caused by deficiency of specific lysosomal enzymes that normally degrade glycoproteins, glycolipids, or mucopolysaccharides. The substances that cannot be catabolized accumulate in lysosomes. Specific enzymes account for specific storage diseases. Included in this group are Gaucher\u2019s, Hurler\u2019s, Tay-Sachs, Niemann-Pick, Fabry\u2019s, Morquio&#8217;s Scheie&#8217;s, and Maroteaux-Lamy disease.<\/p>\n<hr \/>\n<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>Inborn metabolic disorders are a group of conditions, often characterized by the absence of a specific enzyme in the cell&#8217;s lysosomes. This deficiency results in an accumulation of unusual substances inside the cells, leading to tissue damage.<\/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 disease caused by deficiency of specific lysosomal enzymes that normally degrade glycoproteins, glycolipids, or mucopolysaccharides. The substances that cannot be catabolized accumulate in lysosomes. Specific enzymes account for specific storage diseases. Included in this group are Gaucher\u2019s, Hurler\u2019s, Tay-Sachs, Niemann-Pick, Fabry\u2019s, Morquio&#8217;s Scheie&#8217;s, and Maroteaux-Lamy disease. Inborn metabolic disorders are a group of conditions, [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[12],"tags":[],"class_list":["post-182238","post","type-post","status-publish","format-standard","hentry","category-l"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Lysosomal storage disease - Definition of Lysosomal storage disease<\/title>\n<meta name=\"description\" content=\"A disease caused by deficiency of specific lysosomal enzymes that normally degrade glycoproteins, glycolipids, or mucopolysaccharides. The substances that cannot be catabolized accumulate in lysosomes. Specific enzymes account for specific storage diseases. Included in this group are Gaucher\u2019s, Hurler\u2019s, Tay-Sachs, Niemann-Pick, Fabry\u2019s, Morquio&#039;s Scheie&#039;s, and Maroteaux-Lamy disease.Inborn metabolic disorders are a group of conditions, often characterized by the absence of a specific enzyme in the cell&#039;s lysosomes. This deficiency results in an accumulation of unusual substances inside the cells, leading to tissue damage.\" \/>\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\/lysosomal-storage-disease\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Lysosomal storage disease - Definition of Lysosomal storage disease\" \/>\n<meta property=\"og:description\" content=\"A disease caused by deficiency of specific lysosomal enzymes that normally degrade glycoproteins, glycolipids, or mucopolysaccharides. The substances that cannot be catabolized accumulate in lysosomes. Specific enzymes account for specific storage diseases. Included in this group are Gaucher\u2019s, Hurler\u2019s, Tay-Sachs, Niemann-Pick, Fabry\u2019s, Morquio&#039;s Scheie&#039;s, and Maroteaux-Lamy disease.Inborn metabolic disorders are a group of conditions, often characterized by the absence of a specific enzyme in the cell&#039;s lysosomes. 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