Mucopolysaccharidosis VII (MPS7) – Cat
Kodas: K329
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Short description
Mucopolysaccharidosis VII (MPS7) belongs to a group of genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage.
General Information
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.
Included tests
K384 — Mucopolysaccharidosis VII (MPS7) type 2 – Cat
K397 — Mucopolysacchardidosis VII (MPS7) type 3 – Cat
K650 — Mucopolysacchardidosis VII (MPS7) type 1 – Cat
Specifications
| Breeds | All Breeds |
|---|---|
| Organ | NVT |
| Specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
References
Pubmed ID:
Omia ID:
Turnaround information
- 10 working days