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Neuronale Zeroidlipofuszinose (NCL-6) - Schapendoes option-set-443684-checkbox-1 and at an age of

SKU: 12241675212
4.0

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Description

and at an age of 4 years affected dogs are usually completely blind

seizures and central blindness

Generalisierte progressive Retinaatrophien (gPRA) sind eine Gruppe von vererbten Netzhautdystrophien

Mutation: ACADVL gene

although different mutations in the same gene are responsible for the development of the HNPK

Neuronale Zeroidlipofuszinose (NCL-6) - Schapendoes option-set-443684-checkbox-1 and at an age ofNeuronal ceroid lipofuscinosis is a lysosome storage disorder with an autosomal recessive inheritance. It is characterized by intraneuronal accumulation of autofluorescent lipopigments, early neuronal death in the central nervous system, progressive deterioration of cognitive and motor function, epileptic seizures, visual impairment, anxiety and abnormal behaviour. The progressive clinical signs occur early in dogs life and eventually lead to

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