Neuronale Zeroidlipofuszinose (NCL-1) - Cane Corso
Neuronale Zeroidlipofuszinose (NCL-1) - Cane Corso

Neuronal Ceroid Lipofuscinosis (NCL-1) - Cane Corso

Sale price€49,00
SKU: 2700253

Neuronal 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 dog’s 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. The affected dogs usually have to be euthanized due to deterioration of the neurological functions and overall clinical worsening.

Inheritance: autosomal recessive

Mutation: PPT1 gene

Genetic test: The method used for genetic testing is extremely accurate and allows complete differentiation between affected animals, carriers and healthy dogs. DNA testing can be done at any age.

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Do you have any questions, ideas or requests?
We are happy to help you. Whether by email, telephone or in person, we look forward to speaking with you.

Opening hours:

Mon – Fri from 08:00 – 17:00

You can reach us by phone:

Mon – Fri from 10:00 – 12:00 and 14:00 - 16:00

Landline AT: +43 (0) 662 / 43 93 83
Landline DE: +49 (0) 8654 / 68 24 430

You can reach us by email:
support(at)feragen.at

Postal address:

Austria:
FERAGEN GmbH
Laboratory for genetic veterinary diagnostics
Strubergasse 26
5020 Salzburg

Germany:
KUBEOS GmbH
c/o FERAGEN
Niedervillern 8
83410 Running

The German address is a PO box. The samples are forwarded to our laboratory in Austria three times a week.

Please do not send items as "Registered", "Personally delivered", "Registered Mail" or as express mail. This will lead to delays or refusal of acceptance at the PO box.


If you would like one of these shipping options, send the sample directly to us in Austria.