Abstract
A premature infant presented with elevated concentrations of tyrosine in blood and urine, evidence of hepatocellular damage, demineralization of the bones, and a renal Fanconi syndrome. This is the clinical picture found in hereditary tyrosinemia. The infant also had a perinatal infection with cytomegalovirus.
Original language | English (US) |
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Pages (from-to) | 108-112 |
Number of pages | 5 |
Journal | The Journal of pediatrics |
Volume | 92 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1978 |
Externally published | Yes |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health