Mucolipidosis: One of a group of inherited storage diseases in which both lipids and substances called mucopolysaccharides accumulate in the tissues of the body. Four mucolipidosis have been identified: Mucolipidosis I: due to deficiency of the enzyme muramidase. Mucolipidosis II: due to deficiency ...
Found op http://www.medterms.com/script/main/art.html?articlekey=11680
<biochemistry> A group of inherited metabolic diseases characterised by the accumulation of excessive amounts of acid mucopolysaccharides, sphingolipids, and/or glycolipids in visceral and mesenchymal cells. Abnormal amounts of sphingolipids or glycolipids are present in neural tissue. Mental ...
Found op http://www.mondofacto.com/facts/dictionary?mucolipidosis
(mu″ko-lip″ĭ-do´sis) pl. mucolipido´ses any of a group of genetic disorders in which both glycosaminoglycans (GAGs) and lipids accumulate in tissues, but without excess of GAG in the urine. mucolipidosis I sialidosis (type I). mucolipidosis II ...
Found op http://www.encyclo.co.uk/local/21001
mucolipidosis (s), mucolipidoses (pl) any inborn error of metabolism that has clinical and cytologic characteristics of both the mucopolysaccharidoses and the sphingolipidoses.
Found op http://www.wordinfo.info/words/index/info/view_unit/1340/4
Type: Term Pronunciation: myū′kō-lip-i-dō′sis, -sēz Definitions: 1. Any of a group of lysosomal storage diseases in which symptoms of visceral and mesenchymal mucopolysaccharide, glycoprotein, oligosaccharide, or glycolipid storage are present; clinically, they bear a...
Found op http://www.medilexicon.com/medicaldictionary.php?t=56311
Mucolipidosis (ML) is a group of inherited metabolic disorders that affect the body`s ability to carry out the normal turnover of various materials within cells. When originally named, the mucolipidoses derived their name from the similarity in presentation to both mucopolysaccharidoses and sphingo...
Found op http://en.wikipedia.org/wiki/Mucolipidosis
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