Mucopolysaccharidosis type VII (MPS 7)

Mucopolysaccharidosis type VII belongs to a group of rare genetic disorders of glycosaminglycan... more
Заболевание
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.
Порода
бразильский терьер, немецкая овчарка
Тип наследования
autosomal recessive
Длительность теста
1-2 weeks after arrival of the sample in the lab
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