€57,48 €47,50 IVA esclusa
Gangliosidosis, GM2, TYPE II – 3, also known as Sanddhoff disease and GM2 gangliosidosis variant 0, is a lysosomal storage disease in which there is a buildup of GM2 gangliosides (a type of glycolipid) in various tissues.
Working days 10
Specifiche
| Breeds | |
|---|---|
| Gene | |
| Organ | |
| specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
| Mode of Inheritance | |
| Chromosome | |
| Also known as | |
| Year Published |
Informazioni generali
Gangliosidosis, GM2, TYPE II – 3, also known as Sanddhoff disease and GM2 gangliosidosis variant 0, is a lysosomal storage disease in which there is a buildup of GM2 gangliosides (a type of glycolipid) in various tissues.
Caratteristiche cliniche
Cats affected with Gangliosidosis, GM2, TYPE II – 3 show progressive neuromuscular dysfunction and impaired growth from an early age. Affected kittens have head tremors at the beginning followed by impaired coordination of leg movements which eventually lead to paralysis.
Informazioni aggiuntive
Riferimenti
Pubmed ID: 15081585
Omia ID: 1462
Prodotti correlati
-
- Basset Hound, Pembroke Welsh Corgi
- RALY
- Apparato tegumentario
-
- Pug
- MYH9
- Apparati multipli
-
- American Quarter Horse, Thoroughbred
- ITGA2B
- Cardiovascular system
-
- Yorkshire Terrier
- L2HGDH
- Sistema nervoso
