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Perioperative care of a child with non-ketotic hyperglycinemia
Non-ketotic hyperglycinemia (NKGH) is an autosomal recessive disorder of glycine metabolism. Defective glycine cleavage results in elevated concentrations of glycine in plasma, urine and cerebrospinal fluid. The accumulation of glycine, an inhibitory neurotransmitter, leads to a clinical presentatio...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications
2010
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2980668/ https://ncbi.nlm.nih.gov/pubmed/21189859 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1658-354X.71578 |
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