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K397

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

How does it work?

1. Select your product(s)

Select your single test, a CombiBreed Package or create your own Bundle.

2. Collect DNA sample

Collect DNA material as indicated with our products and send it to our laboratory.

3. Results

We handle your DNA sample with care and provide you with the results.

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