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Спадкова ксантинурія

ORPHA:3467· ICD-10 E79.8· Hereditary xanthinuria

Визначення(English summary)

A rare purine metabolism disorder due to inherited deficiency of the xanthine dehydrogenase/oxidase enzyme and is characterized by very low (or undetectable) concentrations of uric acid in blood and urine and very high concentration of xanthine in urine, leading to urolithiasis.

Поширеність
Unknown
Успадкування
Autosomal recessive
Вік початку
All ages