Ketogenic diet, a potentially valuable therapeutic option for the management of refractory epilepsy in classical neonatal nonketotic hyperglycinemia: a case report

Author:

Kava Maina P.,Robertson Annie,Greed Lawrence,Balasubramaniam Shanti

Publisher

Springer Science and Business Media LLC

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Reference13 articles.

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2. Ohya Y, Ochi N, Mizutani N, Hayakawa C, Watanabe K. Nonketotic hyperglycinemia: Treatment with NMDA antagonist and consideration of neuropathogenesis. Pediatr Neurol. 1991;7:65–68.

3. Hennermann JB, Berger JM, Grieben U, Scharer G, Van Hove JL. Prediction of long-term outcome in glycine encephalopathy: a clinical survey. J Inherit Metab Dis. 2012;35:253–61.

4. Swanson MA, Coughlin CR, Scharer GH, Szerlong HJ, Bjoraker KJ, Spector EB, et al. Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia. Ann Neurol. 2015;78:606–18.

5. Jaeken J, de Koning T, van Hove J. Disorders of GABA, glycine, serine and proline. In: Blau N, Duran M, Blaskovics ME, Gibson KM, editors. Physician’s Guide to the Laboratory Diagnosis of Metabolic Diseases. 2nd ed. Berlin: Springer; 2002. p. 123–40.

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