Dihydropyrimidinase Deficiency
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Dihydropyrimidinase Deficiency
General description
A genetic variant in the DPYS gene has been described in a cat in association with dihydropyrimidinase deficiency. This is a disorder of protein metabolism and leads to symptoms such as lethargy and vomiting, which often occur after eating, especially when following a high-protein diet. In addition, the disease can lead to malnutrition. The blood test reveals an elevated ammonia level.
Breeds
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Order details
| Test number | Included only in LABOGeneticsXXL – Cat |
Test specifications
| Inheritance | probably autosomal recessive |
| Gen | DPYS |
| Mutation | G-A |
| References | OMIA:001776-9685 |
