Familial spastic paraplegia, autosomal dominant, 1

Introduction: Familial spastic paraplegia, autosomal dominant, 1

Description of Familial spastic paraplegia, autosomal dominant, 1

Familial spastic paraplegia, autosomal dominant, 1 (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

Familial spastic paraplegia, autosomal dominant, 1: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial spastic paraplegia, autosomal dominant, 1:

• Familial spastic paraplegia
• Spastic paraplegia
• Autosomal dominant
• Autosomal dominant disease
• Autosomal dominant disorder
• Familial
• Familial disorder
• Spastic
• Spastic disorders

Familial spastic paraplegia, autosomal dominant, 1: Rare Disease

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

Familial spastic paraplegia, autosomal dominant, 1 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, 1, or a subtype of Familial spastic paraplegia, autosomal dominant, 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Familial spastic paraplegia, autosomal dominant, 1 as a Disease

Familial spastic paraplegia, autosomal dominant, 1: 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

Familial spastic paraplegia, autosomal dominant, 1: Related Diseases

Familial spastic paraplegia, autosomal dominant, 1: Familial spastic paraplegia, autosomal dominant, 1 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 Familial spastic paraplegia, autosomal dominant, 1 (Spastic paraplegia 3, autosomal dominant)

Some of the symptoms of Familial spastic paraplegia, autosomal dominant, 1 incude:

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

See full list of 7 symptoms of Familial spastic paraplegia, autosomal dominant, 1 (Spastic paraplegia 3, autosomal dominant)

Terms associated with Familial spastic paraplegia, autosomal dominant, 1:

Terms Similar to Familial spastic paraplegia, autosomal dominant, 1:

• SPG3
• SPG3A
• Strumpell disease
• Spastic paraplegia 3, autosomal dominant
• FSP1

Source - NIH

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