Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency (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

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