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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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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications
2010
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| Matèries: | |
| Accés en línia: | 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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