Mucopolysaccharidosis type 6 (ARSB: c.1427T>C + c.1558G>A)
Mucopolysaccharidosis VI is a lysosomal storage disease, the symptoms of which can appear as early as 6 weeks of age. These include facial dysmorphia, reduced flexibility, growth retardation, loss of mobility of posterior limbs, joint problems and corneal opacification.
Transmission
Autosomal recessiveBreed
Ragdoll, Domestic Shorthair , Birman, Oriental Longhair, Oriental Shorthair, Siamese



