Renal tubular dysfunction in multiple acyl-CoA dehydrogenase deficiency

J Inherit Metab Dis. 1997 Aug;20(4):604-5. doi: 10.1023/a:1005371428912.

Authors

A A Morris¹, S E Olpin, W G Van't Hoff, A W Johnson, J V Leonard

Affiliation

¹ Institute of Child Health, London, UK.

PMID: 9266400
DOI: 10.1023/a:1005371428912

No abstract available

Publication types

Case Reports

MeSH terms

Acidosis, Renal Tubular / enzymology
Acidosis, Renal Tubular / genetics
Acidosis, Renal Tubular / physiopathology*
Acyl-CoA Dehydrogenases / deficiency*
Amino Acid Metabolism, Inborn Errors / enzymology
Amino Acid Metabolism, Inborn Errors / genetics
Amino Acid Metabolism, Inborn Errors / physiopathology*
Female
Glutarates / urine
Humans
Infant
Kidney Tubules / physiopathology*

Substances

Glutarates
Acyl-CoA Dehydrogenases