Growth in patients with phenylketonuria
✍ Scribed by J. Weglage; J. H. Brämswig; H. G. Koch; S. Karassalidou; K. Ullrich
- Publisher
- Springer
- Year
- 1994
- Tongue
- English
- Weight
- 229 KB
- Volume
- 153
- Category
- Article
- ISSN
- 0340-6997
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📜 SIMILAR VOLUMES
During routine screening procedures for amino-acid disorders by thin-layer chromatography, a 16-year-old boy was found to have phenylketonuria and cystinuria. A phenylalanine and a cystine loading were carried out. The patient was found to be homozygous for phenylketonuria and heterozygous for cysti
Two patients with phenylketonuria detected by newborn screening for inborn errors of metabolism were treated with low phenylanine formulae. Serum phenylalanine levels were well controlled, but serum glycine levels were elevated until 4 or 5 months of age. This was probable due to the high content of