Sequential magnetic resonance spectroscopic changes in a patient with nonketotic hyperglycinemia
Nonketotic hyperglycinemia (NKH) is a rare inborn error of amino acid metabolism. A defect in the glycine cleavage enzyme system results in highly elevated concentrations of glycine in the plasma, urine, cerebrospinal fluid, and brain, resulting in glycine-induced encephalopathy and neuropathy. The...
Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Korean Pediatric Society
2012-08-01
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Series: | Korean Journal of Pediatrics |
Subjects: | |
Online Access: | http://kjp.or.kr/upload/pdf/kjped-55-301.pdf |