TY - CHAP M1 - Book, Section TI - Iminoglycinuria A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a benign inborn error of metabolism caused by a defect in renal tubular amino acid transport resulting in abnormal urinary excretion of glycine, proline, and hydroxyproline. The clinical manifestations include encephalopathy, mental retardation, deafness, blindness, renal lithiasis, mild to severe hypertension, and cerebral (gyrate) atrophy. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164073712 ER -