Beta-mercaptolactate cysteine disulfiduria

Orpha code: 1035OMIM code: 249650

Definicja

An extremely rare disorder of methionine cycle and sulfur amino acid metabolism characterized by increased urine excretion of beta-mercaptolactate-cysteine disulfide (due to deficiency of mercaptopyruvate sulfurtransferase activity in erythrocytes), leading to a positive cyanide nitroprusside test. Association with intellectual disability, congenital lens dislocation, and behavioral abnormalities has been reported, however the causal link remains to be established. There have been no further descriptions in the literature since 1981.

Disease data
Klasyfikacja

Biological anomaly

Synonimy
3-mercaptopyruvate sulfurtransferase deficiency
Zespół Ampola
Ampola syndrome
MCDU
Kod ORPHA
1035
Kod OMIM
249650
Kod ICD10
E72.1
Kod ICD11
-

No additional description.

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