Calcification of the basal ganglia
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🔬 Metabolic and Endocrine Causes
- Hypoparathyroidism – most common systemic cause
- ↓ PTH → ↓ calcium, ↑ phosphate
- Leads to symmetrical basal ganglia calcifications
- May be idiopathic or post-surgical
- Pseudohypoparathyroidism
- PTH resistance; biochemical profile resembles hypoparathyroidism
- Hyperparathyroidism
- Less common, but can also lead to intracranial calcifications
- Other metabolic disorders
- Hypomagnesemia, hypophosphatasia, mitochondrial cytopathies (like MELAS)
🧬 Genetic and Degenerative Disorders
- Fahr’s Disease (Idiopathic Basal Ganglia Calcification)
- Familial, autosomal dominant
- Progressive neurologic symptoms (parkinsonism, dementia, seizures)
- Normal calcium/phosphorus levels
- Wilson’s Disease
- Copper accumulation → may cause T2 hyperintensities or calcifications
- Neurologic and hepatic involvement
- Mitochondrial disorders
- MELAS, Leigh syndrome
- Often show basal ganglia abnormalities and calcifications
☣️ Toxic/Environmental Causes
- Lead poisoning
- Chronic exposure may lead to calcifications and cognitive/behavioral changes
- Carbon monoxide poisoning
- Hypoxic damage → calcifications of globus pallidus over time
🦠 Infectious Causes
- Congenital infections (especially TORCH):
- Toxoplasmosis, Cytomegalovirus (CMV) – classically cause periventricular or basal ganglia calcifications in neonates
🧠 Others
- Radiation therapy
- Chronic neuroinflammation
🧪 Workup Suggestion (in symptomatic or extensive cases)
- Serum calcium, phosphate, PTH, magnesium
- Vitamin D levels
- Brain CT (best to detect calcifications)
- Consider genetic testing if familial or Fahr’s suspected
- Toxicology screen if exposure suspected