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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Detalles Bibliográficos
Autores principales: Allee, Joy, Tobias, Joseph D.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980668/
https://www.ncbi.nlm.nih.gov/pubmed/21189859
http://dx.doi.org/10.4103/1658-354X.71578

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980668/
https://www.ncbi.nlm.nih.gov/pubmed/21189859
http://dx.doi.org/10.4103/1658-354X.71578

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