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Mucopolysaccharidosis (MPS VII) belongs to a group of genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage.
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Specifications
| Breeds | |
|---|---|
| Gene | |
| Organ | |
| specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
| Mode of Inheritance | |
| Chromosome | |
| Also known as | |
| Year Published |
General information
Mucopolysaccharidosis (MPS VII) belongs to a group of genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage.
Clinical features
Clinical signs are corneal clouding and severe skeletal deformities. Affected cats are unable to ambulate at several weeks to months of age.
Additional information
References
Pubmed ID: 26118695
Omia ID: 667
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