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1. Albrigth syndrome

2. Bilateral striato-pallido-dentate calcinosis

3. Carbonic anhydrase II deficiency

4. Cockayne syndrome

5. Down syndrome

6. Fahr disease

7. Familial progressive encephalopathy with calcification of the basal ganglia (Aicardi-Goutieres syndrome)

8. GM1-gangliosidosis

9. Hallervorden-Spatz disease

10. Hypo-,hyper-parathyreoidism

11. Krabbe leukodystrophy

12. Lipoid proteinosis

13.Nicrocephaly and intracranial calcification

14. Mitochondrial cytopathies

15. Multiple endocrine neoplasia I

16. Neurofibromatosis

17. Pterin defects

     - Dihydropteridine reductase deficiency

     - GTP cyclohydrolase I deficiency

     - 6-pyruvoyletetrahydropterin synthase deficiency

     - Sepiapterin reductase deficiency

     - Spondyloepiphyseal dysplasia