SPG3A

Introduction: SPG3A

Description of SPG3A

SPG3A (medical condition): A an early onset, very slow progressing form of spastic...more »

See also:

Spastic paraplegia 3, autosomal dominant:
  »Introduction: Spastic paraplegia 3, autosomal dominant
  »Symptoms of Spastic paraplegia 3, autosomal dominant

SPG3A: Rare Disease

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

SPG3A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SPG3A, or a subtype of SPG3A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SPG3A as a Disease

SPG3A: Another name for Spastic paraplegia 3, autosomal dominant (or close medical condition association).
  »Introduction: Spastic paraplegia 3, autosomal dominant
  »Symptoms of Spastic paraplegia 3, autosomal dominant

SPG3A: Related Diseases

SPG3A: SPG3A is listed as a type of (or associated with) the following medical conditions in our database:

• Neuromuscular conditions
• Muscle conditions
• Nervous system conditions
• Movement conditions
• Musculoskeletal conditions
• Degenerative conditions
• Lower limb conditions
• Genetic conditions
• Limb conditions

Symptoms of SPG3A (Spastic paraplegia 3, autosomal dominant)

Some of the symptoms of SPG3A incude:

• Progressive walking difficulty
• Lower leg spasticity
• Lower leg weakness
• Sphincter control problems
• Spastic gait

See full list of 7 symptoms of SPG3A (Spastic paraplegia 3, autosomal dominant)

Terms associated with SPG3A:

Terms Similar to SPG3A:

• Strumpell disease
• Spastic paraplegia 3, autosomal dominant
• FSP1
• Familial spastic paraplegia, autosomal dominant, 1
• SPG3

Source - NIH

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