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Dictionary » Alpha-N-acetylgalactosaminidase deficiency, type 1
 

Alpha-N-acetylgalactosaminidase deficiency, type 1

Introduction: Alpha-N-acetylgalactosaminidase deficiency, type 1

Description of Alpha-N-acetylgalactosaminidase deficiency, type 1

Alpha-N-acetylgalactosaminidase deficiency, type 1 (medical condition): Schindler disease is a rare congenital metabolic disorder involving...more »

See also:

Schindler disease, type 1:
  »Introduction: Schindler disease, type 1
  »Symptoms of Schindler disease, type 1
  »Treatments for Schindler disease, type 1

Alpha-N-acetylgalactosaminidase deficiency, type 1: Related Topics

These medical condition or symptom topics may be relevant to medical information for Alpha-N-acetylgalactosaminidase deficiency, type 1:

Alpha-N-acetylgalactosaminidase deficiency, type 1: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Alpha-N-acetylgalactosaminidase deficiency, type 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Alpha-N-acetylgalactosaminidase deficiency, type 1, or a subtype of Alpha-N-acetylgalactosaminidase deficiency, type 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Alpha-N-acetylgalactosaminidase deficiency, type 1 as a Disease

Alpha-N-acetylgalactosaminidase deficiency, type 1: Another name for Schindler disease, type 1 (or close medical condition association).
  »Introduction: Schindler disease, type 1
  »Symptoms of Schindler disease, type 1
  »Treatments for Schindler disease, type 1

Alpha-N-acetylgalactosaminidase deficiency, type 1: Related Diseases

Alpha-N-acetylgalactosaminidase deficiency, type 1: Alpha-N-acetylgalactosaminidase deficiency, type 1 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Alpha-N-acetylgalactosaminidase deficiency, type 1 (Schindler disease, type 1)

Some of the symptoms of Alpha-N-acetylgalactosaminidase deficiency, type 1 incude:

  • Loss of previously acquired physical skills
  • Loss of previously acquired mental abilities
  • Progressive neurological symptoms
  • Muscle weakness
  • Impaired vision

Treatments for Alpha-N-acetylgalactosaminidase deficiency, type 1 (Schindler disease, type 1)

Treatments for Alpha-N-acetylgalactosaminidase deficiency, type 1 (Schindler disease, type 1) include:

  • There is no cure for the disease but symptomatic measures may be utilized e.g. antiseizure medication. Neurologists, ophthalmologists, physical therapist and genetic counselors are usually seen

Treatment of Alpha-N-acetylgalactosaminidase deficiency, type 1: For more treatment information about Alpha-N-acetylgalactosaminidase deficiency, type 1, see treatment of Schindler disease, type 1 (Alpha-N-acetylgalactosaminidase deficiency, type 1)

Alpha-N-acetylgalactosaminidase deficiency, type 1: Related Disease Topics

These medical disease topics may be related to Alpha-N-acetylgalactosaminidase deficiency, type 1:

Terms associated with Alpha-N-acetylgalactosaminidase deficiency, type 1:

Terms Similar to Alpha-N-acetylgalactosaminidase deficiency, type 1:

Source - NIH

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