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you benefit from over 55 additional health tests – with continuous expansions
Mutation: ACADVL gene
rather than a thick and even coat covering the whole body
In our laboratory we test HIVEP3 gene mutation which was demonstrated to be fully penetrant and concordant with clinical signs
wiederholte Bildung subkutaner Hämatome und unerklärliche Lahmheit seit der Geburt
Neuronale Zeroidlipofuszinose (NCL-6) - Schapendoes option-set-443684-checkbox-1 you benefit from over 55Neuronal 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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