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...
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| Main Authors: | , , , , , , , , , , |
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| Format: | Book |
| Published: |
Korean Pediatric Society,
2012-08-01T00:00:00Z.
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