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Dictionary » MPS2
 

MPS2

Introduction: MPS2

Description of MPS2

MPS2 (medical condition): Disorder of mucopolysaccharide metabolism in juveniles.

See also:

Mucopolysaccharidosis II:
  »Introduction: Mucopolysaccharidosis II
  »Symptoms of Mucopolysaccharidosis II
  »Treatments for Mucopolysaccharidosis II

MPS2 as a Disease

MPS2: Another name for Mucopolysaccharidosis II (or close medical condition association).
  »Introduction: Mucopolysaccharidosis II
  »Symptoms of Mucopolysaccharidosis II
  »Treatments for Mucopolysaccharidosis II

MPS2: Related Diseases

MPS2: MPS2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of MPS2 (Mucopolysaccharidosis II)

Some of the symptoms of MPS2 incude:

See full list of 12 symptoms of MPS2 (Mucopolysaccharidosis II)

Treatments for MPS2 (Mucopolysaccharidosis II)

Treatments for MPS2 (Mucopolysaccharidosis II) include:

Read more about treatments for MPS2

Treatment of MPS2: For more treatment information about MPS2, see treatment of Mucopolysaccharidosis II (MPS2)

MPS2: Article Excerpts about Mucopolysaccharidosis II

MPS II, also called Hunter syndrome, affects juveniles and includes a mild and a severe form. Signs of the severe form are joint stiffness, mental deterioration, dwarfing, and progressive deafness. Death usually occurs by age 15. Symptoms of the mild form include short stature, limitation of motion, and features such as an enlarged forehead, lips, and tongue and misaligned teeth. (Source: excerpt from NINDS Mucopolysaccharidoses Information Page: NINDS)

MPS2: Related Disease Topics

These medical disease topics may be related to MPS2:

Interesting Medical Articles:

Medical dictionaries:

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