Neuronale Zeroidlipofuszinose (NCL-1) - Cane Corso Hundebesitzer führen wir die gewünschte Zusatzanalyse

führen wir die gewünschte Zusatzanalyse durch

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

thromboembolic events and renal failure

Juvenile myoclonic epilepsy (JME) is a breed-specific generalized myoclonic epilepsy with an early onset

Mundschleimhaut oder 1-2 ml EDTA-Blut

Neuronale Zeroidlipofuszinose (NCL-1) - Cane Corso Hundebesitzer führen wir die gewünschte ZusatzanalyseNeuronal 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.