Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-19T15:31:57.341Z Has data issue: false hasContentIssue false
  • English
  • Français

The Physiognomic, Psychometric, Behavioral and Neurological Aspects of Phenylketonuria

Published online by Cambridge University Press:  08 February 2018

Frederick Edward Kratter
Frederick Edward Kratter*
Affiliation:
Letchworth Village, Thiells, N. Y., U.S.A.
Get access Rights & Permissions [Opens in a new window]

Extract

Phenylketonuria is an inborn metabolic disorder affecting the body's ability to hydroxylate phenylalanine to tyrosine.

Its incidence in the general population has been estimated at 0.004 per cent. and its institutional frequency at approximately 0.2 to 0.9 per cent.

Type
Original Articles
Information
Journal of Mental Science , Volume 105 , Issue 439 , April 1959 , pp. 421 - 427
Copyright
Copyright © Royal College of Psychiatrists, 1959 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Alvord, E. C. Jr., et al., J. Neuropath. and Exper. Neurol. 1950, 9, 298.CrossRefGoogle Scholar
Jervis, G. A., “A contribution to the Study of the Influence of Heredity on Mental Deficiency”, J. Psychol. Asthenics., 1939, 44, 2, 13–24.Google Scholar
Wright, S. W., “Phenylketonuria”, J. Amer. Med. Ass., 165, No. 16, 21 December, 1957.CrossRefGoogle ScholarPubMed
Submit a response

eLetters

No eLetters have been published for this article.