SCA18

Introduction: SCA18

Description of SCA18

SCA18 (medical condition): A rare genetic disorder (chromosome 7q22-31 defect) characterized...more »

See also:

Spinocerebellar ataxia 18:
  »Introduction: Spinocerebellar ataxia 18
  »Symptoms of Spinocerebellar ataxia 18

SCA18 as a Disease

SCA18: Another name for Spinocerebellar ataxia 18 (or close medical condition association).
  »Introduction: Spinocerebellar ataxia 18
  »Symptoms of Spinocerebellar ataxia 18

SCA18: Related Diseases

SCA18: SCA18 is listed as a type of (or associated with) the following medical conditions in our database:

• Degenerative conditions
• Brain conditions
• Head conditions
• Nervous system conditions
• Coordination and balance conditions
• Movement conditions
• Spinal cord conditions
• Back conditions
• Genetic conditions
• Neuromuscular conditions
• Muscle conditions
• Musculoskeletal conditions

Symptoms of SCA18 (Spinocerebellar ataxia 18)

Some of the symptoms of SCA18 incude:

• Gait ataxia
• Mild sensory neuropathy
• Speech problems
• Walking problems
• Sensory loss

See full list of 15 symptoms of SCA18 (Spinocerebellar ataxia 18)

SCA18: Related Disease Topics

These medical disease topics may be related to SCA18:

• progressive neurodegenerative disease
• genetic disorder
• Machado-Joseph disease
• nystagmus
• ataxia
• seizures
• hand tremor
• macular degeneration

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