Deficiency of 5‐oxoprolinase in an 8‐year‐old with developmental delay
- 1 May 1996
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 19 (3) , 367-368
- https://doi.org/10.1007/bf01799269
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- 5‐Oxoprolinase deficiency associated with severe psychomotor developmental delay, failure to thrive, microcephaly and microcytic anaemiaJournal of Inherited Metabolic Disease, 1995
- 5‐Oxoprolinuria associated with 5‐oxoprolinase deficiency; further evidence that this is a benign disorderJournal of Inherited Metabolic Disease, 1993
- Pyroglutamic aciduria (5‐Oxoprolinuria) without glutathione synthetase deficiency and with decreased pyroglutamate hydrolase activityJournal of Inherited Metabolic Disease, 1981
- 5‐OXOPROLINURIA DUE TO HEREDITARY 5‐OXOPROLINASE DEFICIENCY IN TWO BROTHERS–A NEW INBORN ERROR OF THE γ‐GLUTAMYL CYCLEActa Paediatrica, 1981