SPG13

Introduction: SPG13

Description of SPG13

SPG13 (medical condition): A rare genetic disorder characterized mainly by...more »

See also:

Spastic paraplegia 13, autosomal dominant:
  »Introduction: Spastic paraplegia 13, autosomal dominant
  »Symptoms of Spastic paraplegia 13, autosomal dominant

SPG13: Rare Disease

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

SPG13 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SPG13, or a subtype of SPG13, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SPG13 as a Disease

SPG13: Another name for Spastic paraplegia 13, autosomal dominant (or close medical condition association).
  »Introduction: Spastic paraplegia 13, autosomal dominant
  »Symptoms of Spastic paraplegia 13, autosomal dominant

SPG13: Related Diseases

SPG13: SPG13 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 SPG13 (Spastic paraplegia 13, autosomal dominant)

Some of the symptoms of SPG13 incude:

• Absent Babinski sign
• Increased arm reflexes
• Progressive lower leg spasticity
• Progressive lower leg weakness
• Progressive lower arm spasticity

See full list of 6 symptoms of SPG13 (Spastic paraplegia 13, autosomal dominant)

Terms associated with SPG13:

Terms Similar to SPG13:

• Spastic paraplegia 13, autosomal dominant

Source - NIH

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