Abstract
A case of failure to thrive in an infant with persistently raised urinary levels of homovanillic and vanillylmandelic acids is descirbed. No neural crest tumour was discovered at surgical exploration or at necropsy. The relation of this biochemical abnormality and failure to thrive is unclear.
Full text
PDF


Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Gitlow S. E., Mendlowitz M., Wilk E. K., Wilk S., Wolf R. L., Bertani L. M. Excretion of catecholamine catabolites by normal children. J Lab Clin Med. 1968 Oct;72(4):612–620. [PubMed] [Google Scholar]
- Hannaway P. J. Failure to thrive: a study of 100 infants and children. Clin Pediatr (Phila) 1970 Feb;9(2):96–99. doi: 10.1177/000992287000900214. [DOI] [PubMed] [Google Scholar]
- ILLINGWORTH R. S. The child who will not thrive. Br J Clin Pract. 1963 May;17:291–296. [PubMed] [Google Scholar]
- LUZZATTI L. FAILURE TO THRIVE. A DIAGNOSTIC APPROACH. Postgrad Med. 1964 Mar;35:270–278. doi: 10.1080/00325481.1964.11695049. [DOI] [PubMed] [Google Scholar]
- Moskowitz M. A., Wurtman R. J. Catecholamines and neurologic diseases (second of two parts). N Engl J Med. 1975 Aug 14;293(7):332–338. doi: 10.1056/NEJM197508142930705. [DOI] [PubMed] [Google Scholar]
- Voorhess M. L. Urinary catecholamine excretion by healthy children. I. Daily excretion of dopamine, norepinephrine, epinephrine, and 3-methoxy-4-hydroxymandelic acid. Pediatrics. 1967 Feb;39(2):252–257. [PubMed] [Google Scholar]

