Macrocephaly as the presenting feature ofl‐2‐hydroxyglutaric aciduria in a 5‐month‐old boy
- 1 May 1996
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 19 (3), 369-370
- https://doi.org/10.1007/bf01799270
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- l‐2‐Hydroxyglutaric acidaemia: Clinical and biochemical findings in 12 patients and preliminary report onl‐2‐hydroxyacid dehydrogenaseJournal of Inherited Metabolic Disease, 1993
- l‐2‐Hydroxyglutaric aciduria: Two further casesJournal of Inherited Metabolic Disease, 1993
- L‐2‐Hydroxyglutaric aciduria: an inborn error of metabolism?Journal of Inherited Metabolic Disease, 1980