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Dictionary » Familial spastic paraplegia, autosomal dominant 3
 

Familial spastic paraplegia, autosomal dominant 3

Introduction: Familial spastic paraplegia, autosomal dominant 3

Description of Familial spastic paraplegia, autosomal dominant 3

Familial spastic paraplegia, autosomal dominant 3 (medical condition): A rare genetic disorder characterized by progressive leg...more »

See also:

Spastic paraplegia 6, autosomal dominant:
  »Introduction: Spastic paraplegia 6, autosomal dominant
  »Symptoms of Spastic paraplegia 6, autosomal dominant

Familial spastic paraplegia, autosomal dominant 3: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial spastic paraplegia, autosomal dominant 3:

Familial spastic paraplegia, autosomal dominant 3: Rare Disease

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

Familial spastic paraplegia, autosomal dominant 3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Familial spastic paraplegia, autosomal dominant 3, or a subtype of Familial spastic paraplegia, autosomal dominant 3, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Familial spastic paraplegia, autosomal dominant 3 as a Disease

Familial spastic paraplegia, autosomal dominant 3: Another name for Spastic paraplegia 6, autosomal dominant (or close medical condition association).
  »Introduction: Spastic paraplegia 6, autosomal dominant
  »Symptoms of Spastic paraplegia 6, autosomal dominant

Familial spastic paraplegia, autosomal dominant 3: Related Diseases

Familial spastic paraplegia, autosomal dominant 3: Familial spastic paraplegia, autosomal dominant 3 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Familial spastic paraplegia, autosomal dominant 3 (Spastic paraplegia 6, autosomal dominant)

Some of the symptoms of Familial spastic paraplegia, autosomal dominant 3 incude:

  • Abnormal gait
  • Increased reflexes in lower legs
  • Lower leg spasticity
  • Weak hip flexion
  • Weak ankle movements

Terms associated with Familial spastic paraplegia, autosomal dominant 3:

Terms Similar to Familial spastic paraplegia, autosomal dominant 3:

Source - NIH

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