5‐OXOPROLINURIA DUE TO HEREDITARY 5‐OXOPROLINASE DEFICIENCY IN TWO BROTHERS–A NEW INBORN ERROR OF THE γ‐GLUTAMYL CYCLE

Abstract

ABSTRACT. Larsson, A., Mattsson, B., Wauters, E. A. K., van Gool, J. D., Duran, M. and adman, S. K. (Department of Paediatrics, Karolinska Institute, St. Goran's Children's Hospital, Stockholm, Sweden, and University Children's Hospital, “Het Wilhelmina Kinderziekenhuis”, Utrecht, The Netherlands). 5‐Oxoprolinuria due to 5‐oxoproIinase deficiency in two brothers–a new inborn error of the γ‐glutamyl cycle. Acta Paediatr Scand, 70:301, 1981.–Two brothers, aged 16 and 11 years, had recurrent episodes of vomiting, diarrhoea and abdominal pain, starting in infancy. In spite of extensive investigations no cause of their enterocolitis could be established. After several years symptomatic treatment was discontinued without any recurrence of symptoms. Their father and several paternal relatives have had kidney stones. Both boys developed urolithiasis and an oxalate‐containing stone was removed from the elder brother's kidney. He had no hypercalciuria. His glomerular and tubular function tests were normal. Gas chromatography of urine from both brothers revealed massive excretion of L‐5‐oxoproline (pyroglutamic acid). Glutathione levels in erythrocytes of both patients were normal. The activities of enzymes of the γ‐glutamyl cycle were analysed in erythrocytes, leukocytes and cultured skin fibroblasts. The level of glutathione synthetase was normal, as was the affinity of this enzyme for its substrate γ‐glutamyl‐cysteine. Feedback inhibition of γ‐glutamyl‐cysteine synthetase by glutathione was also normal. Both patients had a specific deficiency of 5‐oxoprolinase, the activity of which was 2‐A % of that of control subjects. Their parents had intermediate 5‐oxoprolinase activities in fibroblasts, indicating a recessive mode of inheritance. Thus, 5‐oxoprolinuria in these two patients was due to a lack of S‐oxoprolinase, i.e., a new inborn error in the γ‐glutamyl cycle.