Hunter syndrome history and symptoms

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Hunter syndrome Microchapters

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Overview

Historical Perspective

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Pathophysiology

Causes

Differentiating Hunter syndrome from other Diseases

Epidemiology and Demographics

Risk Factors

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Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

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Overview

The symptoms of Hunter syndrome (MPS II) are generally not apparent at birth, but usually start to become noticeable after the first year of life. Often, the first symptoms of Hunter syndrome may include inguinal hernias, ear infections, runny noses, and colds. Since these symptoms are quite common among all infants, they are not likely to lead a doctor to make a diagnosis of Hunter syndrome right away. As the buildup of GAG continues throughout the cells of the body, signs of Hunter syndrome become more visible.

History and Symptoms

Juvenile Form

It is the early-onset and severe form of the disease.

  • Aggressive behavior
  • Hyperactivity
  • Decreased mental function
  • Severe mental retardation
  • Spasticity

Late Form

  • Mild to no mental deficiency

Common Features

References

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