Difference between revisions of "Pyruvate dehydrogenase phosphatase 1 deficiency"

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Pyruvate dehydrogenase phosphatase 1 deficiency is a [[genetic diseases of dogs|genetic]] storage disease characterized by dramatic exercise intolerance and post exercise collapse.
 
Pyruvate dehydrogenase phosphatase 1 deficiency is a [[genetic diseases of dogs|genetic]] storage disease characterized by dramatic exercise intolerance and post exercise collapse.
  

Revision as of 05:17, 26 November 2012

Pyruvate dehydrogenase phosphatase 1 deficiency is a genetic storage disease characterized by dramatic exercise intolerance and post exercise collapse.

Pyruvate Dehydrogenase Phosphatase 1 is a global mitochondrial enzyme which reverses the effects of pyruvate dehydrogenase kinase upon pyruvate dehydrogenase, affecting glycolysis (phosphorylase and phosphofructokinase deficiency) and fatty acid oxidation (palmitoyl carnitine transferase deficiency)[1].

This disease is mainly reported in the Clumber Spaniel and Sussex Spaniel and clinical symptoms are primarily exercise intolerance.

Diagnosis is by PCR assays.

Dietary restriction may be beneficial in some dogs, as well as limit exercise to lash walks[2].

References

  1. Cameron JM et al (2009) Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype. Hum Genet 125(3):319-326
  2. Cameron JM et al (2007) Identification of a canine model of pyruvate dehydrogenase phosphatase 1 deficiency. Mol Genet Metab 90(1):15-23