Epilepsy of infancy with migrating focal seizures in a patient with nonketotic hyperglycinemia
Nonketotic hyperglycinemia (NKH) is an inborn error of glycine metabolism leading to refractory epilepsy and severe developmental delays. It is caused by autosomal recessive inheritance of a defect in the glycine cleavage system in the mitochondrial enzymatic complex pathway [1]. This defect le...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | en |
| Published: |
Korean Child Neurology Society
2022
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| Subjects: | |
| Online Access: | http://irep.iium.edu.my/104286/2/104286_Epilepsy%20of%20Infancy%20with%20Migrating%20Focal%20Seizures.pdf http://irep.iium.edu.my/104286/ https://www.annchildneurol.org/journal/view.php?doi=10.26815/acn.2022.00346 |
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