Iminoglycinuria meaning

ĭm′ə-nō-glī′sə-no͝or ē-ə
A benign inborn error of amino acid transport, causing glycine, proline, and hydroxyproline to be excreted in the urine.
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(medicine) A rare autosomal-recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine and the imino acids proline and hydroxyproline, resulting in excess urinary excretion of all three acids.
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