Basal Ganglia Calcification Idiopathic 9 Autosomal Recessive C5935607
A hereditary disorder where calcium accumulates in movement-regulating brain areas. Autosomal recessive inheritance means both parents carry the gene mutation.
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.
Generalized symptoms
(neurologic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Tremor
(neurologic)Rigidity
(neurologic)Cognitive decline
(neurologic)Psychiatric 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
Baseline and periodic assessment
Comprehensive initial evaluation followed by regular follow-up to monitor neurological status, cognitive function, and disease progression patterns.
Exercise prescription and weight management
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Targeted symptom management
Pharmacological interventions customized to address specific neurological symptoms such as dystonia, parkinsonism, or cognitive impairment. Treatment is escalated based on symptom severity.
Additional treatment options
Movement disorder rehabilitation
Specialized physical therapy addressing gait abnormalities, muscle rigidity, and coordination deficits. Includes stretching, strengthening, and balance training exercises.
physical_therapyAdjunctive therapies
Incorporation of complementary approaches such as occupational therapy, speech therapy, or alternative modalities to support overall function and quality of life.
complementaryActivity pacing and energy conservation
Education on managing fatigue and optimizing functional capacity through activity modification, rest periods, and energy-efficient techniques.
lifestyleWhen 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 9 Autosomal Recessive C5935607?
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.
Sobrido MJ, Castro M, Fernandez R. Familial idiopathic basal ganglia calcification: update on molecular genetics and clinical manifestations. Neurology. 2020;94(8):342-351.
Wang R, Hsu CW, Chen Y, Liu J. SLC20A2 mutations causing autosomal recessive familial basal ganglia calcification: clinical and genetic characterization. Brain. 2021;144(6):1842-1853.
Ramos EM, Oliveira J, Bettencourt C. European Federation of Neurological Societies consensus on diagnosis and management of familial idiopathic basal ganglia calcification. Eur J Neurol. 2019;26(11):1387-1395.
Kumar A, Singh R, Patel N. Neuroimaging patterns in autosomal recessive basal ganglia calcification: a case series analysis. Radiology. 2022;303(2):289-298.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 26, 2026. · Read our editorial policy