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Mutation: COL4A5-Gen
Inheritance: X-linked recessive
which include retinal thinning
Reduction of genetic risks
Gentest: Die Methode
Neuronale Zeroidlipofuszinose 10 (NCL-10) ISAG Mutation: COL4A5-GenNeuronal ceroid lipofuscinoses (NCLs) are a group of heritable 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
