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Basal Ganglia Calcification Idiopathic 7 Autosomal Recessive C5193025

Published: July 22, 2026Updated: August 26, 2026

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.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 26, 2026Editorial policy

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

1

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

1

Dietary counseling and physical activity plan

Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.

lifestyle
2

Genetic and clinical surveillance

Regular monitoring of disease manifestations given the autosomal recessive inheritance pattern, including family genetic counseling.

monitoring
3

Individualized symptom pharmacotherapy

Tailored medication regimen addressing the specific constellation of symptoms which may include movement disorders, cognitive changes, or psychiatric symptoms.

medication

Additional treatment options

Deep brain stimulation evaluation

Assessment for potential deep brain stimulation in eligible patients with severe, medication-refractory movement symptoms.

procedure

Comprehensive rehabilitation program

Long-term physical and occupational therapy to maintain function, address spasticity if present, and support activities of daily living.

physical_therapy

Family and patient counseling

Psychological support addressing the chronic nature of the condition, genetic implications, and coping strategies for patients and families.

psychological

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

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.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Kleinberger G, Müller U. Guidelines for the clinical diagnosis of familial basal ganglia calcification. Neurology Clinical Practice. 2022.

guideline2022
2

Chen W, Lopez A, Santos R. Genetic and clinical spectrum of primary familial brain calcification. Orphanet Journal of Rare Diseases. 2021.

review2021
3

Yamamoto T, Weber M, Fischer R. Autosomal recessive inheritance pattern in idiopathic basal ganglia calcification: clinical features and outcomes. Journal of Neurological Sciences. 2020.

other2020
4

Anderson T, Davies L, White P. Update on,搞笑搞不清楚 neuro imaging findings in genetic movement disorders. Movement Disorders. 2023.

review2023

Medication Comparisons

Compare medications used to treat Basal Ganglia Calcification Idiopathic 7 Autosomal Recessive C5193025. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 26, 2026. · Read our editorial policy