Phenylketonuria occurs in approximately one out of ev ery 100,000 American Negro births.
This report of a Negro child with the disease care fully outlines her diagnosis, treatment, and physical and mental progress. Emphasized also is the need for even more widespread screening programs.
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References
1.
Graw, R.G. and Koch, R.: Phenylketonuria in two American Negroes. Amer. J. Dis. Child.114: 412, 1967.
Hassan, M.M. : Phenylketonuria in a Sudanese family. J. Pediat.64: 282, 1964.
4.
Jervis, G.: The genetics of phenylpyruvic oligophrenia. J. Ment. Sci.85: 719, 1939.
5.
Stadler, H., Meyer. H. and Leland, H.: Phenylpyruvic oligophrenia in a mulatto. J. Nerv. Ment. Dis.124: 205, 1956.
6.
Katz, H.P. and Menckes, J.H.: Phenylketonuria occurring in an American Negro. J. Pediat.65: 71, 1964.
7.
Newman, H.A. and Engel, L.: Phenylketonuria in a Negro infant . J. Pediat.67: 329, 1965.
8.
Guthrie, R. and Whitney, S.: Phenylketonuria detection in the newborn infant as a routine hospital procedure. Chidlren'sBureau Publication No. 419, U. S. Department of Health, Education and Welfare, 1964.
9.
Folling, A.: Uker Ausscheidung von Phenylbrenztrauhen saure in der Harn als Stoffwechselanomalie in Verkindung mit Imbezillist. Z. Physiol. Chem.227: 169, 1934.
10.
Bechel, H., Gerrard, J. and Hickmans, E.M.: Influence of phenylalanine intake on phenylketonuria. Lancet2: 812, 1953.
11.
Hsia, D.Y.-Y. , Berman, J.L. and Slates, H.M.: Screening newborn infants for phenylketonuria . JAMA188: 203, 1964.
12.
Rosser, P.L. : Personal communication.
13.
Glass, B. and Li, C.: The dynamics of radial-intermixture—an analysis based on the American Negro. Amer. J. Human Gen.5: 1, 1953.
14.
Bessman, S.P. : Legislation and advances in medical knowledge— acceleration or inhibition. J. Pediat.69: 334, 1966.
15.
Symposium on treatment of amino acid disorders. Amer. J. Dis. Child.113: 2, 1966.