Lethal multiple acyl‐CoA dehydrogenation deficiency with dysmorphic features
- 1 March 1987
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 10 (1) , 95-96
- https://doi.org/10.1007/bf01799495
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- PRENATAL DIAGNOSIS OF DYSMORPHIC NEONATAL-LETHAL TYPE II GLUTARICACIDURIAThe Lancet, 1984
- Glutaric acidemia type II: A form with deleterious intrauterine effectsThe Journal of Pediatrics, 1983
- Multiple Acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothersEuropean Journal of Pediatrics, 1982
- Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothersEuropean Journal of Pediatrics, 1982
- Glutaric aciduria Type IIThe Journal of Pediatrics, 1980