Mucopolysachharidose de type VII (MPS 7)

Mucopolysaccharidosis type VII belongs to a group of rare genetic disorders of glycosaminglycan...plus
Disease
Mucopolysaccharidosis type VII belongs to a group of rare genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage. Clinical signs are corneal clouding and severe skeletal deformities. Affected dogs are unable to ambulate at several weeks to months of age.
Breed
Berger allemand, Terrier brésilien
Heredity
autosomal recessive
Test duration
1-2 weeks after arrival of the sample in the lab
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