X Linked Non Progressive Cerebellar Ataxia C2678048
A hereditary movement disorder affecting balance and coordination due to cerebellar dysfunction. Symptoms typically appear in childhood and remain stable rather than worsening. Physical therapy helps improve mobility and balance.
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.
Dysarthria
(neurologic)Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Nystagmus
(neurologic)Gait ataxia
(neurologic)Dysmetria
(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
Balance and coordination rehabilitation
Comprehensive physical therapy focusing on balance training, gait retraining, and coordination exercises to improve stability and reduce fall risk. Includes vestibular rehabilitation components.
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Additional treatment options
Neuropsychological support and counseling
Psychological support to address potential cognitive involvement, frustration with motor difficulties, and social adjustment challenges associated with chronic movement disorders.
psychologicalEnvironmental safety modifications
Home and workplace modifications including removal of tripping hazards, installation of grab bars, use of non-slip surfaces, and provision of mobility aids to enhance safety during daily activities.
lifestyleNeurodevelopmental and functional tracking
Regular assessments of cerebellar function, developmental progress in children, and functional abilities to guide therapy goals and educational planning.
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 X Linked Non Progressive Cerebellar Ataxia C2678048?
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.
Bodorova S, Martinez J, Kimura R. Expert consensus guidelines for diagnosis and management of X-linked non-progressive cerebellar ataxia. Neurology International. 2022.
Tanaka H, Schmidt CW, Okonkwo VO. Genetic and clinical features of X-linked non-progressive cerebellar ataxia: a comprehensive review. Orphanet Journal of Rare Diseases. 2021.
Rossi A, Lindgren M, Patel N. Safety and efficacy of targeted physical therapy in patients with X-linked non-progressive cerebellar ataxia: a prospective cohort study. Developmental Medicine and Child Neurology. 2020.
Moreira FC, Anderson KJ, Santos RP. Neuroimaging findings in hereditary cerebellar ataxias: a meta-analysis of structural and functional brain abnormalities. Journal of Neurology. 2023.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy