{"id":107178,"date":"2021-05-20T06:03:35","date_gmt":"2021-05-20T06:03:35","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=107178"},"modified":"2021-05-27T04:56:14","modified_gmt":"2021-05-27T04:56:14","slug":"pompes-disease","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/pompes-disease\/","title":{"rendered":"Pompe&#8217;s disease"},"content":{"rendered":"<p>A rare genetic disease due to a mutation in the gene for the enzyme \u03b1-1,- glucosidase; characterized by excess glycogen stores in the muscle. Also called Type II glycogen storage disease.<\/p>\n<hr \/>\n<p>Pompe disease (PD) is a rare, heritable disorder of carbohydrate metabolism. PD is typified by glycogen (a complex carbohydrate polymer) deposition in skeletal and heart muscle, which causes progressive weakness, loss of muscle mass, and failure of the heart\u2019s pumping action.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A rare genetic disease due to a mutation in the gene for the enzyme \u03b1-1,- glucosidase; characterized by excess glycogen stores in the muscle. Also called Type II glycogen storage disease. Pompe disease (PD) is a rare, heritable disorder of carbohydrate metabolism. PD is typified by glycogen (a complex carbohydrate polymer) deposition in skeletal 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":[16],"tags":[],"class_list":["post-107178","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>Pompe&#039;s disease - Definition of Pompe&#039;s disease<\/title>\n<meta name=\"description\" content=\"A rare genetic disease due to a mutation in the gene for the enzyme \u03b1-1,- glucosidase; characterized by excess glycogen stores in the muscle. Also called Type II glycogen storage disease.Pompe disease (PD) is a rare, heritable disorder of carbohydrate metabolism. PD is typified by glycogen (a complex carbohydrate polymer) deposition in skeletal and heart muscle, which causes progressive weakness, loss of muscle mass, and failure of the heart\u2019s pumping action.\" \/>\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\/pompes-disease\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Pompe&#039;s disease - Definition of Pompe&#039;s disease\" \/>\n<meta property=\"og:description\" content=\"A rare genetic disease due to a mutation in the gene for the enzyme \u03b1-1,- glucosidase; characterized by excess glycogen stores in the muscle. Also called Type II glycogen storage disease.Pompe disease (PD) is a rare, heritable disorder of carbohydrate metabolism. 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