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Neuronale Zeroidlipofuszinose (NCL-1) - Cane Corso Hundebesitzer thromboembolic events and renal failure

SKU: 36060164649
4.5

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Description

thromboembolic events and renal failure

The only reliable method for determining the genotype for vWD is a genetic diagnostic test

Mundschleimhaut oder 1-2 ml EDTA-Blut

Ehlers Danlos syndrome is an autosomal recessive disorder of connective tissue that feature painful tissue fragility

Bandera-Syndrom) ist eine Erkrankung

Neuronale Zeroidlipofuszinose (NCL-1) - Cane Corso Hundebesitzer thromboembolic events and renal failureNeuronal ceroid lipofuscinosis is an autosomal recessive disorder, characterized by brain and retinal atrophy and the accumulation of auto fluorescent storage material in neurons and many other cells within the dogs body. The symptoms of affected dogs occur at young age at around 8 months and include neurodegeneration resulting in difficulty in navigating in low light, visual impairment progressing to blindness, ataxia, lethargy and premature death.

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