SCA20

Introduction: SCA20

Description of SCA20

SCA20 (medical condition): A rare genetic disorder (chromosome 11 defect) characterized by palatal tremor...more »

See also:

Spinocerebellar ataxia 20:
  »Introduction: Spinocerebellar ataxia 20
  »Symptoms of Spinocerebellar ataxia 20

SCA20 as a Disease

SCA20: Another name for Spinocerebellar ataxia 20 (or close medical condition association).
  »Introduction: Spinocerebellar ataxia 20
  »Symptoms of Spinocerebellar ataxia 20

SCA20: Related Diseases

SCA20: SCA20 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
• Neuromuscular conditions
• Muscle conditions
• Genetic conditions
• Musculoskeletal conditions

Symptoms of SCA20 (Spinocerebellar ataxia 20)

Some of the symptoms of SCA20 incude:

• Gait ataxia
• Mild sensory neuropathy
• Speech problems
• Dysphonia
• Ataxia

See full list of 8 symptoms of SCA20 (Spinocerebellar ataxia 20)

SCA20: Related Disease Topics

These medical disease topics may be related to SCA20:

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

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Unspecified congenital anomaly of digestive system

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