[Non-ketotic hyperglycinemia]. / Non-ketoticus hyperglycinaemia.
Orv Hetil
; 136(5): 245-9, 1995 Jan 29.
Article
em Hu
| MEDLINE
| ID: mdl-7772127
ABSTRACT
Three children with non-ketotic hyperglycinaemia (NKH) is reported. Two patients had typical neonatal form of NKH, one patients had atypical form of NKH. The clinical symptoms laboratory findings and therapeutical approach are discussed. One of the patients with typical neonatal form of NKH is died, neuropatological examination revealed corpus callosal agenesis and diffuse hypomyelinisation. The two children treated with N-methyl-D-aspartate-antagonist drugs reached a significantly better clinical condition. The authors reviewed the data of the literature, especially focused on the therapeutical possibilities.
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Base de dados:
MEDLINE
Assunto principal:
Erros Inatos do Metabolismo dos Aminoácidos
/
Glicina
Idioma:
Hu
Ano de publicação:
1995
Tipo de documento:
Article