The E.E.G. in non-ketotic hyperglycinaemia (author's transl)

12 cases of non-ketotic hyperglycinemia in neonates diagnosed at a time of neurological distress were studied. A characteristic tracing was observed permitting correct diagnosis in 6 cases. It consisted of a burst suppression characterized by high voltage complexes separated by low amplitude sequenc...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Revue d'électroencéphalographie et de neurophysiologie clinique 1978-01, Vol.8 (1), p.102
Hauptverfasser:	Mises, J, Moussali-Salefranque, F, Plouin, P, Temam, G, Saudubray, J M
Format:	Artikel
Sprache:	fre
Schlagworte:	Amino Acid Metabolism, Inborn Errors - physiopathology Brain Diseases, Metabolic - physiopathology Cerebral Cortex - physiopathology Child Electroencephalography Female Glycine - blood Humans Male
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	12 cases of non-ketotic hyperglycinemia in neonates diagnosed at a time of neurological distress were studied. A characteristic tracing was observed permitting correct diagnosis in 6 cases. It consisted of a burst suppression characterized by high voltage complexes separated by low amplitude sequences. This appearance remained until the 15th day, with no electroclinical changes. In cases followed the trace closely resembled hypsarrhythmia.
ISSN:	0370-4475