Pyruvatdehydrogenasedefizienz (PDP1)
Pyruvatdehydrogenasedefizienz (PDP1)

Pyruvate Dehydrogenase Deficiency (PDP1)

Sale price€49,00
SKU: 2700307

Exercise intolerance syndromes in humans and animals are well known to be associated with inborn errors of metabolism affecting glycolysis and fatty acid oxidation. PDP1 is a hereditary disease in Clumber and Sussex Spaniels. Disease is caused by deficiency of pyruvate dehydrogenase phosphatase 1, an enzyme that activates the pyruvate dehydrogenase complex. This enzyme complex is presented in every cell of the body and is involved in energy production.

PDP1 deficiency in Clumber and Sussex Spaniels clinically appears in 1 year as an exercise intolerance. Proper diet rich in fats and low in sugar can control disease progression. Without this diet, affected dogs will die within a few years of age. Some studies also suggest that PDP1 deficiency causes high numbers of neonatal deaths and deaths shortly after birth.

Inheritance: autosomal recessive

Mutation: PDP1 gene

Genetic test: The method used for testing is extremely accurate and allows complete differentiation between affected animals, carriers and healthy dogs. Testing can be done at any age.

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Opening hours:

Mon – Fri from 08:00 – 17:00

You can reach us by phone:

Mon – Fri from 10:00 – 12:00 and 14:00 - 16:00

Landline AT: +43 (0) 662 / 43 93 83
Landline DE: +49 (0) 8654 / 68 24 430

You can reach us by email:
support(at)feragen.at

Postal address:

Austria:
FERAGEN GmbH
Laboratory for genetic veterinary diagnostics
Strubergasse 26
5020 Salzburg

Germany:
KUBEOS GmbH
c/o FERAGEN
Niedervillern 8
83410 Running

The German address is a PO box. The samples are forwarded to our laboratory in Austria three times a week.

Please do not send items as "Registered", "Personally delivered", "Registered Mail" or as express mail. This will lead to delays or refusal of acceptance at the PO box.


If you would like one of these shipping options, send the sample directly to us in Austria.