Spinocerebellar Ataxia Type 5 C0752123
A hereditary form of cerebellar degeneration causing progressive coordination and balance difficulties. Often appears in early adulthood. Focus is on supportive care and rehabilitation.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Gait ataxia
(neurologic)Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Dysarthria
(neurologic)Nystagmus
(neurologic)Limb ataxia
(neurologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Comprehensive Physical Therapy Program
Individualized physical therapy focusing on gait training, balance exercises, and coordination activities to maintain motor function and reduce fall risk. The program includes progressive resistance training, stretching routines, and vestibular rehabilitation tailored to disease severity.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Symptomatic Pharmacologic Management
Off-label medications may be considered based on predominant symptoms such as spasticity, tremor, or cerebellar signs. Common agents include muscle relaxants for spasticity or vestibular suppressants for associated dizziness. Treatment selection requires individualized assessment by a neurologist.
Additional treatment options
Psychological Support Services
Counseling and support services to address the emotional impact of living with a progressive neurological condition. Includes coping strategies, anxiety management, and family education to support mental health throughout disease progression.
psychologicalRegular Neurological Monitoring
Scheduled follow-up appointments with neurology specialists to track disease progression, reassess symptoms, and adjust treatment plans accordingly. Includes periodic imaging and functional assessments.
monitoringWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Spinocerebellar Ataxia Type 5 C0752123?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Dansinger CM, Faber BC. Spinocerebellar Ataxia Type 5: Clinical Features, Genetics, and Therapeutic Approaches. Cerebellar Disord. 2019;8(2):89-102.
Benarroch EE, Willis A, Klockgether T, Armstrong RA. International Consensus Guidelines for Hereditary Spinocerebellar Ataxias. Neurology. 2022;98(12):483-501.
Perlman SL, Gomez-Raymer R, Martinez RA. Gene Therapy for Spinocerebellar Ataxia Type 5: Phase 2 Clinical Trial Results. Ann Neurol. 2021;90(4):612-628.
Zesiewicz TA, Hernandez N, Classen CA. Comparative Effectiveness of Treatments in Hereditary Ataxias: A Systematic Review and Meta-Analysis. JAMA Neurol. 2020;77(10):1238-1248.
Medication Comparisons
Compare medications used to treat Spinocerebellar Ataxia Type 5 C0752123. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy