{"id":108779,"date":"2021-05-27T07:32:28","date_gmt":"2021-05-27T07:32:28","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=108779"},"modified":"2021-05-27T07:32:28","modified_gmt":"2021-05-27T07:32:28","slug":"nonketotic-hyperglycinemia","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/nonketotic-hyperglycinemia\/","title":{"rendered":"Nonketotic hyperglycinemia"},"content":{"rendered":"<p>Nonketotic hyperglycinemia (NKH) is a rare autosomal- recessive trait involving an error of glycine metabolism. Large amounts of the amino acid glycine accumulate in the body fluids, particularly in the cerebrospinal fluid. Two subtypes of this disorder exist: nonclassic NKH and neonatal NKH. The former appears later in life and presents with milder neurological deficits and varying degrees of mental retardation.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Nonketotic hyperglycinemia (NKH) is a rare autosomal- recessive trait involving an error of glycine metabolism. Large amounts of the amino acid glycine accumulate in the body fluids, particularly in the cerebrospinal fluid. Two subtypes of this disorder exist: nonclassic NKH and neonatal NKH. The former appears later in life and presents with milder neurological deficits [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[14],"tags":[],"class_list":["post-108779","post","type-post","status-publish","format-standard","hentry","category-n"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Nonketotic hyperglycinemia - Definition of Nonketotic hyperglycinemia<\/title>\n<meta name=\"description\" content=\"Nonketotic hyperglycinemia (NKH) is a rare autosomal- recessive trait involving an error of glycine metabolism. Large amounts of the amino acid glycine accumulate in the body fluids, particularly in the cerebrospinal fluid. Two subtypes of this disorder exist: nonclassic NKH and neonatal NKH. The former appears later in life and presents with milder neurological deficits and varying degrees of mental retardation.\" \/>\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\/nonketotic-hyperglycinemia\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Nonketotic hyperglycinemia - Definition of Nonketotic hyperglycinemia\" \/>\n<meta property=\"og:description\" content=\"Nonketotic hyperglycinemia (NKH) is a rare autosomal- recessive trait involving an error of glycine metabolism. Large amounts of the amino acid glycine accumulate in the body fluids, particularly in the cerebrospinal fluid. Two subtypes of this disorder exist: nonclassic NKH and neonatal NKH. 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