This is a Multisystem condition.

Mucopolysaccharidosis IIIB, Sanfilippo Syndrome Type B, MPS IIIB

What is MPS IIIB?

The mucopolysaccharidoses (MPS) are a group of hereditary lysosomal storage disorders in which specific glycosaminoglycans (GAGs) accumulate in lysosomes. Mucopolysaccharidosis III is characterized by lysosomal accumulation of the GAG heparan sulphate (HS). Unlike other forms of MPS, MPS III causes a progressive and primarily neurological disease.

What are the signs & symptoms that develop in affected dogs?

Affected dogs develop a slowly progressive ataxia, typically leading to humane euthanasia before six years of age. Other signs include mental dullness, with exaggerated abnormal gait (hypermetria), truncal swaying (pulling the spine and attached tissues back and forth), and fine whole-body and head tremors.

When do signs and symptoms develop?

Clinical signs may be observed at approximately two years of age.

How do vets diagnose this condition?

Diagnosis is made based on clinical history, physical examination, genetic testing, and ruling out other causes of similar symptoms. Intracytoplasmic granules may be found in the white cells of peripheral blood and cerebrospinal fluid (CSF), and increased HS may be measured in plasma, CSF, and urine of affected dogs.

How is this condition treated?

There is no cure for MPS IIIB; all currently available treatments are symptomatic or supportive in nature. Gene therapy and enzyme replacement therapy are evolving fields that require more research to be available clinically.

What actions should I take if my dog is affected?

  • Please give your dog any medication as prescribed by your veterinarian.
  • Keeping your affected dog comfortable at home is the best therapy you can provide.
  • Slings can be used to assist with their mobility, and caution should be taken to avoid falling hazards.
Shopping in the {{ userRegion }}?

You're viewing our {{ region }} website, but it looks like you're in the {{ userRegion }}.

Visit {{ market }} site