Transient neonatal hyperglycinemia
โ Scribed by Raphael Schiffmann; Edward M. Kaye; John K. Willis III; Diane Africk; Mary Ampola
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 331 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
โฆ Synopsis
Two patients with neonatal seizures and subsequent normal neurological development were found to have nonketotic hyperglycinemia In both patients, hyperglycinemia resolved at 6 weeks of age. After cerebrospinal References fluid glycine levels were normalized, the seizures
๐ SIMILAR VOLUMES
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