Miller-Dieker syndrome (type I lissencephaly) with specific EEG changes

Miller-Dieker syndrome (type I lissencephaly) with specific EEG changes

We present the case report of a girl with a subtype of Lissencephaly syndrome, type I, "Miller-Dieker syndrome", pointing out the specific EEG features in infancy and early childhood. The following pathognomonic EEG manifestations may confirm the diagnosis of an lissencephalic syndrome: ab...

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Veröffentlicht in:Monatsschrift Kinderheilkunde 1990-09, Vol.138 (9), p.615-618
Hauptverfasser: Wörle, H, Keimer, R, Köhler, B
Format: Artikel
Sprache:ger
Schlagworte:
Agenesis of Corpus Callosum
Cerebral Cortex - abnormalities
Echoencephalography
Electroencephalography
Evoked Potentials - physiology
Female
Fetal Growth Retardation - diagnosis
Humans
Infant, Newborn
Microcephaly - diagnosis
Spasms, Infantile - diagnosis
Syndrome
Tomography, X-Ray Computed
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Beschreibung
Zusammenfassung:We present the case report of a girl with a subtype of Lissencephaly syndrome, type I, "Miller-Dieker syndrome", pointing out the specific EEG features in infancy and early childhood. The following pathognomonic EEG manifestations may confirm the diagnosis of an lissencephalic syndrome: abnormally fast background activity of an extraordinary high voltage increasing with age, missing topographic structuring, no reactivity to sleep or medication, unusually high-voltaged sharp-slow-wave complexes.
ISSN:0026-9298