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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Ketogenic diet in a patient with congenital hyperinsulinism: a novel approach to prevent brain damage

Fig. 2

Comparison between cerebral activity and glycemia before and after 1 year of KD. Disappearance of absence epilepsy or electrical signs despite hypoglycemia. Before KD, long monitoring EEG showed generalized spike and waves discharges with loss of contact during hypoglycemia. On KD, long monitoring EEG appeared normal, with absence of ictal EEG and epileptic manifestations even during hypoglycemia

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172