NCL-D - Neuronal Ceroid Lipofuscinosis/English Setter

Race liée: 

Nervous system degeneration

Description: 
Neurodegenerative disease leading to loss of motor function and vision and to behavioural disorder
Symptomes: 
Progressive loss of motor function and coordination, behavioural disorder, blanks, progressive loss of vision
Age d'aparition: 
Between 12 and 18 months old
Fréquence: 
_
Gène impliqué: 
CLN8
Mutation testée: 
c.491T>C
Transmission: 
Autosomal Recessive
Brevet: 
_
Remarques: 
_