Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings

Eur J Pediatr. 1982 Sep;139(1):56-9. doi: 10.1007/BF00442081.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Cerebral Cortex / abnormalities*
  • Fibroblasts / metabolism
  • Glutarates / urine
  • Humans
  • Infant, Newborn
  • Male
  • Metabolism, Inborn Errors / genetics*
  • Polycystic Kidney Diseases / genetics*

Substances

  • Glutarates