{"id":201199,"date":"2022-12-27T05:29:56","date_gmt":"2022-12-27T05:29:56","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=201199"},"modified":"2022-12-27T05:29:56","modified_gmt":"2022-12-27T05:29:56","slug":"sphingolipidosis","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/sphingolipidosis\/","title":{"rendered":"Sphingolipidosis"},"content":{"rendered":"

Any disease marked by a defective metabolism of sphingolipids. These genetically determined errors of metabolism include Sandhoffs disease, Fabry\u2019s disease, Tay-Sachs disease, Kufs\u2019 disease, Gaucher\u2019s disease, Krabbe\u2019s leukodystrophy, Niemann-Pick disease, Batten disease, and Spielmeyer-Vogt disease. They are marked by neurological deterioration, usually beginning a few months after birth and eventually leading to death except in the adult form of Gaucher\u2019s disease. These diseases can be detected by examining fluid obtained by amniocentesis.<\/p>\n

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Any disease marked by a defective metabolism of sphingolipids. These genetically determined errors of metabolism include Sandhoffs disease, Fabry\u2019s disease, Tay-Sachs disease, Kufs\u2019 disease, Gaucher\u2019s disease, Krabbe\u2019s leukodystrophy, Niemann-Pick disease, Batten disease, and Spielmeyer-Vogt disease. They are marked by neurological deterioration, usually beginning a few months after birth and eventually leading to death except in […]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[19],"tags":[],"class_list":["post-201199","post","type-post","status-publish","format-standard","hentry","category-s"],"yoast_head":"\nSphingolipidosis - Definition of Sphingolipidosis<\/title>\n<meta name=\"description\" content=\"Any disease marked by a defective metabolism of sphingolipids. These genetically determined errors of metabolism include Sandhoffs disease, Fabry\u2019s disease, Tay-Sachs disease, Kufs\u2019 disease, Gaucher\u2019s disease, Krabbe\u2019s leukodystrophy, Niemann-Pick disease, Batten disease, and Spielmeyer-Vogt disease. They are marked by neurological deterioration, usually beginning a few months after birth and eventually leading to death except in the adult form of Gaucher\u2019s disease. These diseases can be detected by examining fluid obtained by amniocentesis.\" \/>\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\/sphingolipidosis\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sphingolipidosis - Definition of Sphingolipidosis\" \/>\n<meta property=\"og:description\" content=\"Any disease marked by a defective metabolism of sphingolipids. These genetically determined errors of metabolism include Sandhoffs disease, Fabry\u2019s disease, Tay-Sachs disease, Kufs\u2019 disease, Gaucher\u2019s disease, Krabbe\u2019s leukodystrophy, Niemann-Pick disease, Batten disease, and Spielmeyer-Vogt disease. 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