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Mucopolysaccharidosis type 2 Hunter syndrome- mild form

Mucopolysaccharidosis type 2 Hunter syndrome- mild form: Introduction

Mucopolysaccharidosis type 2 Hunter syndrome- mild form: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (iduronidate 2-sulfatase) needed to break it down. More detailed information about the symptoms, causes, and treatments of Mucopolysaccharidosis type 2 Hunter syndrome- mild form is available below.

Symptoms of Mucopolysaccharidosis type 2 Hunter syndrome- mild form

Wrongly Diagnosed with Mucopolysaccharidosis type 2 Hunter syndrome- mild form?

Mucopolysaccharidosis type 2 Hunter syndrome- mild form: Related Patient Stories

Mucopolysaccharidosis type 2 Hunter syndrome- mild form: Deaths

Read more about Deaths and Mucopolysaccharidosis type 2 Hunter syndrome- mild form.

Mucopolysaccharidosis type 2 Hunter syndrome- mild form: Complications

Review possible medical complications related to Mucopolysaccharidosis type 2 Hunter syndrome- mild form:

Causes of Mucopolysaccharidosis type 2 Hunter syndrome- mild form

Read more about causes of Mucopolysaccharidosis type 2 Hunter syndrome- mild form.

Disease Topics Related To Mucopolysaccharidosis type 2 Hunter syndrome- mild form

Research the causes of these diseases that are similar to, or related to, Mucopolysaccharidosis type 2 Hunter syndrome- mild form:

Less Common Symptoms of Mucopolysaccharidosis type 2 Hunter syndrome- mild form

Prognosis for Mucopolysaccharidosis type 2 Hunter syndrome- mild form

Prognosis for Mucopolysaccharidosis type 2 Hunter syndrome- mild form: may survive to 7th decade

Mucopolysaccharidosis type 2 Hunter syndrome- mild form: Broader Related Topics

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