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N-acetyl-alpha-D-galactosaminidase: Introduction

N-acetyl-alpha-D-galactosaminidase: 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). More detailed information about the symptoms, causes, and treatments of N-acetyl-alpha-D-galactosaminidase is available below.

Symptoms of N-acetyl-alpha-D-galactosaminidase

  • Telangiectasia
  • Excess urinary sialylglycoaminoacids
  • Warty discolorations on skin
  • Mildly coarse facial features
  • Mild intellectual impairment
  • more symptoms...»

Causes of N-acetyl-alpha-D-galactosaminidase

Read more about causes of N-acetyl-alpha-D-galactosaminidase.

Statistics for N-acetyl-alpha-D-galactosaminidase

N-acetyl-alpha-D-galactosaminidase: Broader Related Topics

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Definitions 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)

Related N-acetyl-alpha-D-galactosaminidase Info

Videos about N-acetyl-alpha-D-galactosaminidase


More information about N-acetyl-alpha-D-galactosaminidase

  1. N-acetyl-alpha-D-galactosaminidase: Introduction
  2. Symptoms
  3. Causes
  4. Treatments

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