Basal Ganglia Calcification Idiopathic 7 Autosomal Recessive C5193025
A rare genetic disorder causing calcium deposits in brain regions that control movement. Inherited in an autosomal recessive pattern, it may lead to movement disorders and neurological symptoms.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Seizures
Generalized symptoms
(neurologic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Parkinsonism
(neurologic)Dystonia
(neurologic)Neuropsychiatric symptoms
(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
Dietary counseling and physical activity plan
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Genetic and clinical surveillance
Regular monitoring of disease manifestations given the autosomal recessive inheritance pattern, including family genetic counseling.
Individualized symptom pharmacotherapy
Tailored medication regimen addressing the specific constellation of symptoms which may include movement disorders, cognitive changes, or psychiatric symptoms.
Additional treatment options
Deep brain stimulation evaluation
Assessment for potential deep brain stimulation in eligible patients with severe, medication-refractory movement symptoms.
procedureComprehensive rehabilitation program
Long-term physical and occupational therapy to maintain function, address spasticity if present, and support activities of daily living.
physical_therapyFamily and patient counseling
Psychological support addressing the chronic nature of the condition, genetic implications, and coping strategies for patients and families.
psychologicalWhen 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 Basal Ganglia Calcification Idiopathic 7 Autosomal Recessive C5193025?
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.
Kleinberger G, Müller U. Guidelines for the clinical diagnosis of familial basal ganglia calcification. Neurology Clinical Practice. 2022.
Chen W, Lopez A, Santos R. Genetic and clinical spectrum of primary familial brain calcification. Orphanet Journal of Rare Diseases. 2021.
Yamamoto T, Weber M, Fischer R. Autosomal recessive inheritance pattern in idiopathic basal ganglia calcification: clinical features and outcomes. Journal of Neurological Sciences. 2020.
Anderson T, Davies L, White P. Update on，搞笑搞不清楚 neuro imaging findings in genetic movement disorders. Movement Disorders. 2023.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 26, 2026. · Read our editorial policy