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Bulletin of the National Research Centre

Table 1 Secondary basal ganglia calcifications. Adapted from Tai and Batla (2015)

From: Neuroradiological findings in a young patient bearing a new single mitochondrial gene mutation (case report)

Endocrinopathies

Hypoparathyroidism, hyperparathyroidism

Inherited

Mitochondrial diseases, Cockayne syndrome, Pantothenate kinase-associated neurodegeneration (PKAN)

Birth hypoxia

 

Infections

TORCH, tuberculosis, AIDS, toxoplasmosis

Toxic

Carbon monoxide or lead poisoning, radiotherapy, chemotherapy

Age-related

 
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