Definition of Sialidosis. Meaning of Sialidosis. Synonyms of Sialidosis

Here you will find one or more explanations in English for the word Sialidosis. Also in the bottom left of the page several parts of wikipedia pages related to the word Sialidosis and, of course, Sialidosis synonyms and on the right images related to the word Sialidosis.

Definition of Sialidosis

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Meaning of Sialidosis from wikipedia

- classified as a sialidosis, it is sometimes referred to as sialidosis type II.[citation needed] A rarer form of sialidosissialidosis type 1 – occurs...
- syndrome Shwartzman phenomenon Shy–Drager syndrome Sialadenitis Sialidosis type 1 and 3 Sialidosis Sialuria, French type Sickle cell anemia Sideroblastic anemia...
- 'protective protein'). Mutations in this gene can lead to sialidosis. Mutations in NEU1 leads to sialidosis, a rare lysosomal storage disease. Sialidase has also...
- Nonkeratan-sulfate-excreting Morquio syndrome Pituitary tumors (adult) Sialidosis type II (congenital) Sialidosis type II (infantile) Sialuria syndrome Simpson–Golabi–Behmel...
- genes Differential diagnosis Other progressive myoclonic epilepsies (sialidosis, myoclonic epilepsy with ragged red fibers, Unverricht-Lundborg disease)...
- (Sly syndrome) Type IX (hyaluronidase deficiency) Mucolipidosis Type I (sialidosis) Type II (I-cell disease) Type III (pseudo-Hurler polydystrophy / phosphotransferase...
- presence or absence of some enzymes related to the sialic acid metabolism. Sialidosis and Sialic acid deficiency with mutations in the NANS gene (see below)...
- gangliosidoses Metachromatic leukodystrophy Niemann–Pick disease Sandhoff disease Sialidosis Congenital developmental diseases (e.g., Leber's congenital amaurosis)...
- therapeutic strategies have been used to replace gene effects while in Sialidosis enzyme replacement therapy has been studied in mouse models. In Lafora's...
- and IV) were historically labeled as mucolipidoses. However, type I (sialidosis) is now classified as a glycoproteinosis, and type IV (Mucolipidosis type...