SPG10

Introduction: SPG10

Description of SPG10

SPG10 (medical condition): An extremely mild form of lower leg spasticity and weakness. Most sufferers...more »

See also:

Spastic paraplegia 10, autosomal dominant:
  »Introduction: Spastic paraplegia 10, autosomal dominant
  »Symptoms of Spastic paraplegia 10, autosomal dominant

SPG10: Rare Disease

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

SPG10 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SPG10, or a subtype of SPG10, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SPG10 as a Disease

SPG10: Another name for Spastic paraplegia 10, autosomal dominant (or close medical condition association).
  »Introduction: Spastic paraplegia 10, autosomal dominant
  »Symptoms of Spastic paraplegia 10, autosomal dominant

SPG10: Related Diseases

SPG10: SPG10 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
• Limb conditions
• Degenerative conditions
• Lower limb conditions
• Genetic conditions

Symptoms of SPG10 (Spastic paraplegia 10, autosomal dominant)

Some of the symptoms of SPG10 incude:

• Spastic gait
• Increased lower leg reflexes

Read more about symptoms of SPG10 (Spastic paraplegia 10, autosomal dominant)

Terms associated with SPG10:

Terms Similar to SPG10:

• Spastic paraplegia 10, autosomal dominant
• Autosomal dominant spastic paraplegia

Source - NIH

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