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Symptoms and Symptom Management Click on a link below to learn more about the specific symptoms of MPS I and how they are managed. General Physical AppearanceNervous System Skeletal System Respiratory System Auditory System Cardiovascular System Ocular System Gastrointestinal System Initial Signs of MPS I MPS I is associated with pathologic effects in most tissue types. Symptoms of MPS I show a chronic and progressive course; they are multisystemic in nature and include corneal clouding, valvular heart disease, joint stiffness, organomegaly (enlarged liver or spleen), and dysostosis multiplex (abnormally shaped bones). 0-6 months: chronic rhinitis, recurrent otitis media or “glue ear,” umbilical or inguinal hernia, above normal growth and head size 6 months – 12 years: facial dysmorphisms, hepatosplenomegaly, skeletal deformities, joint stiffness, developmental delay, corneal clouding, chronic rhinitis, recurrent otitis media or “glue ear” 12+ years: corneal clouding, joint stiffness, valvular heart disease Symptom Management Current treatment of MPS I disease is largely symptomatic. Generally speaking, supportive or symptomatic management can improve the quality of life for affected individuals and their families. |
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