N-acetyl-alpha-D-galactosaminidase (medical condition): A very rare enzyme deficiency (N-acetyl-alpha-D-galactosaminidase) which can occur in three forms: type I (infantile-onset neuroaxonal dystrophy), type II or Kanzaki disease (adult-onset) and type III (mild or moderate form).
See also:
N-acetyl-alpha-D-galactosaminidase:
»Introduction: N-acetyl-alpha-D-galactosaminidase
»Symptoms of N-acetyl-alpha-D-galactosaminidase
N-acetyl-alpha-D-galactosaminidase is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that N-acetyl-alpha-D-galactosaminidase, or a subtype of N-acetyl-alpha-D-galactosaminidase,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
N-acetyl-alpha-D-galactosaminidase (medical condition): See N-acetyl-alpha-D-galactosaminidase (disease information).
»Introduction: N-acetyl-alpha-D-galactosaminidase
»Symptoms of N-acetyl-alpha-D-galactosaminidase
Source - NIH
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