Canine Primary Hyperoxaluria Type I (PH I)

47.90 € inc. Vat

Acronyms: PH I
Gene: AXGT
Mutation: Point mutation
Mode of inheritance: Autosomal recessive
Breeds: Coton de Tulear

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Product Description

Canine Primary Hyperoxaluria Type I (PH I)

Canine primary hyperoxaluria type I (PH I) is a rare, inherited disorder of glyoxylate metabolism affecting the Coton Tulear dog breed. PH I is a form of wider group of primary hyperoxalurias, which are known to affect humans, dogs and cats. Hyperoxaluria is a condition in which oxalate concentrations in the urine are extremely high, which causes kidney damage. Primary hyperoxaluria is a disease caused by genetic mutation, in which the liver produces too much oxalate. Primary hyperoxalurias consist of three main types, each associated with specific metabolic defects. From them, type I is the most common and most severe one with a rapid progression. 80% of cases of primary hyperoxaluria are caused by Type I, which has an early age of onset.

Characteristics and Symptoms

Oxalate is a small molecule naturally present in human or animal body from food intake or as an end product of metabolism reactions, such as the metabolism of certain proteins or the metabolism of vitamin C. However, oxalate is not used within the body for anything, nor degraded, so it needs to be excreted through the urine or feces. In the bladder, oxalate can bind with calcium and form insoluble crystals, which are the most common cause of kidney stones in human patients (75%). Stones can be renal and bladder and they may cause secondary infection of urine, urinary obstruction, and kidney damage, all followed with severe and acute pain. Oxalate deposits may develop in the bones, joints and bone marrow. In severe cases, primary hyperoxaluria type I may cause aneamia and thrombocytopaenia.

In affected dogs, symptoms occur at age of 3 to 4 weeks in form of sudden illness causing inappetence, vomiting, lethargy, decreased urine production, abdominal pain, blood in the urine and death. After development of first symptoms, in time frame of 2 months affected dogs die or get euthanized due to humane reasons. The necropsy reveals numerous oxalate crystals present in the tubules in the renal cortex and at the corticomedullary junction.


Causative mutation of the primary hyperoxaluria type I (PH I) in Coton de Tulears is in the AGXT gene.

Canine primary hyperoxaluria type I (PH I) is inherited as an autosomal recessive disorder. Dog carrying one copy of the mutated gene is heterozygous and will not show the PH I symptoms. When mating two carriers (heterozygotes) at conception each cub has a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier.


Vidgren G, Vainio-Siukola K, Honkasalo S, Dillard K, Anttila M, Vauhkonen H.: Primary hyperoxaluria in Coton de Tulear. Anim Genet. 2012 Jun; 43(3):356-61.