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Encephalopathy due to sulfite oxidase deficiency

MONDO:0019358

Encephalopathy due to sulfite oxidase deficiency is a rare neurometabolic disorder characterized by seizures, progressive encephalopathy and lens dislocation.

39 clinical trials for this condition and its sub-types.

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Sub-types

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (1) Isolated sulfite oxidase deficiency (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1 (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2 (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C (0)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Eye disorder (97) Inborn errors of metabolism (42) Human disease (14) Lens disorder (10) Developmental defect during embryogenesis (7) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2)
Trials to join now! 22 Not yet recruiting 3 Not yet finished but already full! 5 Completed 8 Terminated 1
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