Ophthalmological Findings of Phenylketonuria: A Survey of 14 Cases

Author:

Cotticelli L,Costagliola C,Rinaldi E,DiMeo A,Sartorio R,Vajro P,Andria G

Publisher

SLACK, Inc.

Subject

Ophthalmology,General Medicine,Pediatrics, Perinatology and Child Health

Reference16 articles.

1. 1. Jervis GA: Phenylpyruvic oligophrenia: deficiency of phenylalanine oxidizing system. Proc Soc Exp Biol Med 1953; 82:514.

2. 2. Penrose LS: Two cases of phenylpyruvic amentia. Lancet 1935; 1:23.

3. 3. Blomquist HK Gustavson KH Holmgren G: Severe mental retardation in five siblings due to maternal phenylketonuria. Neuropediatrics 1980; 11:256.

4. 4. Knox WE: Phenylketonuria in Stambury JB Wyngaarden JB Friedricson DS (eds): The metabolic basis of inherited disease ed 3. New York McGraw-Hill Book Co 1972 ? 266.

5. 5. Bertoni G Santabrogio S Giovannini M et al: Phenylketonuria: ophthalmological and clinical problems of assessment in J. Francois - M. Maione (ed): Pediatric Ophthalmology. Chichester (Sussex) and Verona (Italy) John Wiley & Sons Ltd and Cortina Verona Sri 1982 ? 227.

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