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Mucopolysaccharidosis VII (MPS7) belongs to a group of genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage.
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Spezifikationen
| Breeds | |
|---|---|
| Organ | |
| specimen | Tupfer, EDTA Blut, Heparin Blut, Sperma, Gewebe |
Allgemeine Informationen
Mucopolysaccharidosis VII (MPS7) belongs to a group of genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage.
Clinical signs are corneal clouding and severe skeletal deformities. Affected cats are unable to ambulate at several weeks to months of age.
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