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Cystathioninuria
rareCystathioninuria 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.
- Identifiers
- MONDO:0009058 OMIM:219500Orphanet:212
- Causal genes
- CTH
- Part of
- Inborn disorder of amino acid metabolismInborn disorder of methionine cycle and sulfur amino acid metabolism
- Also known as
- cystathionase deficiency · cystathioninuria (disease) · gamma-cystathionase deficiency
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