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Neuronale Zeroidlipofuszinose (NCL-8) - Australian Shepherd-Typ evg-analysen die der Best'schen Makuladystrophie beim

SKU: 22085375489
4.6

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Description

die der Best'schen Makuladystrophie beim Menschen ähnelt

Mutation: VSP13B gene

die klinische Anzeichen verursachten

which is described as the canine moustache and eyebrows

It is caused by axonal swelling in the cerebellum and abnormalities in the brain stem

Neuronale Zeroidlipofuszinose (NCL-8) - Australian Shepherd-Typ evg-analysen die der Best'schen Makuladystrophie beimNeuronal ceroid lipofuscinosis (NCLs) are a group of hereditary diseases, characterized by progressive neuronal degeneration and the accumulation of autofluorescent cytoplasmic inclusions in the brain, retina, and other tissues. Clinical symptoms and progress of the disease include increased rates of irritability, with the possibility of outbursts of aggression, hallucinations, hyperactivity and seizures. Most animals lose their ability to coordinate

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