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Cystathioninuria

MONDO:0009058

Cystathioninuria is an autosomal recessive disorder caused by cystathionine gamma-lyase deficiency. It is usually pyridoxine-dependent, but in very rare cases it may be non-dependent. It is generally considered to be a benign condition without pathogenic relevance. However, association of cystathioninuria with intellectual impairment has been reported in several cases.

Also known as: cystathionase deficiency, cystathioninuria, cystathioninuria (disease), gamma-cystathionase deficiency

1 clinical trial for this condition and its sub-types, 0 tagged with Cystathioninuria itself.

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