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Erschienen in: Journal of Inherited Metabolic Disease 3/2010

01.06.2010 | Images in Metabolic Medicine

Basal ganglia lesions in the early stage of Menkes disease

verfasst von: Katarina Koprivsek, Milos Lucic, Dusko Kozic, Maja Djordjevic, Ruzica Kravljanac

Erschienen in: Journal of Inherited Metabolic Disease | Ausgabe 3/2010

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Excerpt

An 11-month-old boy presented with progressive truncal hypotonia with poor head control and myoclonic seizures. His hair was sparse and stiff, his skin hypopigmented. Magnetic resonance imaging (MRI) (Fig. 1) demonstrated slight volume loss of the supratentorial white matter, symmetrical T2-weighted (T2W) hyperintense signal of the putamens and isolated round lesions of the left caudate head. The basal ganglia lesions showed restricted diffusion on diffusion-weighted imaging (DWI) (Fig. 2). Light microscopy of the boy’s hair demonstrated pili torti. Low levels of plasma copper and caeruloplasmin confirmed the diagnosis of Menkes disease.
Literatur
Zurück zum Zitat Bindu PS, Sinha S, Taly AB et al (2007) Menkes syndrome presenting as myoclonic seizures: neuroimaging and EEG observations. J Child Neurol 22:452–455CrossRefPubMed Bindu PS, Sinha S, Taly AB et al (2007) Menkes syndrome presenting as myoclonic seizures: neuroimaging and EEG observations. J Child Neurol 22:452–455CrossRefPubMed
Zurück zum Zitat Arita JH, Faria EC, Peruci MM et al (2009) Menkes disease as a differential diagnosis of child abuse. Arq Neuropsiquiatr 67:507/9 Arita JH, Faria EC, Peruci MM et al (2009) Menkes disease as a differential diagnosis of child abuse. Arq Neuropsiquiatr 67:507/9
Metadaten
Titel
Basal ganglia lesions in the early stage of Menkes disease
verfasst von
Katarina Koprivsek
Milos Lucic
Dusko Kozic
Maja Djordjevic
Ruzica Kravljanac
Publikationsdatum
01.06.2010
Verlag
Springer Netherlands
Erschienen in
Journal of Inherited Metabolic Disease / Ausgabe 3/2010
Print ISSN: 0141-8955
Elektronische ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-010-9063-0

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