[Phenylketonuria undiagnosed, unrecognizable and neglected. Review of failures in diagnosis, therapy, and prevention of hereditary disorders of phenylalanine]

Cesk Pediatr. 1987 Mar;42(3):134-8.
[Article in Czech]
No abstract available

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Diagnosis, Differential
  • Humans
  • Infant
  • Infant, Newborn
  • Phenylketonurias* / diagnosis
  • Phenylketonurias* / prevention & control
  • Phenylketonurias* / therapy