Seitelberger disease

Introduction: Seitelberger disease

Description of Seitelberger disease

Seitelberger disease (medical condition): An inherited disorder involving progressive muscular and...more »

See also:

Neuroaxonal dystrophy, infantile:
  »Introduction: Neuroaxonal dystrophy, infantile
  »Symptoms of Neuroaxonal dystrophy, infantile

Seitelberger disease: Rare Disease

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

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

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Seitelberger disease as a "rare disease".

Source - Orphanet

Seitelberger disease as a Disease

Seitelberger disease: Another name for Neuroaxonal dystrophy, infantile (or close medical condition association).
  »Introduction: Neuroaxonal dystrophy, infantile
  »Symptoms of Neuroaxonal dystrophy, infantile

Seitelberger disease: Related Diseases

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

• Infant health conditions
• Nervous system conditions
• Degenerative conditions

Symptoms of Seitelberger disease (Neuroaxonal dystrophy, infantile)

Some of the symptoms of Seitelberger disease incude:

• Incontinence during sleep
• Progressive speech deterioration
• Rapid involuntary eye movements
• Crossed eyes
• Blindness

See full list of 36 symptoms of Seitelberger disease (Neuroaxonal dystrophy, infantile)

Terms associated with Seitelberger disease:

Terms Similar to Seitelberger disease:

• Neuroaxonal dystrophy, infantile
• INAD
• Infantile neuroaxonal dystrophy

Source - NIH

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