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dc.contributor.authorJohn B. Bodensteiner
dc.contributor.authorG. Bradley Schaefer
dc.contributor.authorGina M. Keller
dc.contributor.authorJames N. Thompson
dc.contributor.authorMary K. Bowen
dc.date.accessioned2016-01-14T19:53:15Z
dc.date.accessioned2016-03-30T15:31:50Z
dc.date.available2016-01-14T19:53:15Z
dc.date.available2016-03-30T15:31:50Z
dc.date.issued1997-09-01
dc.identifier.citationBodensteiner, J. B., Schaefer, G. B., Keller, G. M., Thompson, J. N., & Bowen, M. K. (1997). Macrocerebellum: Neuroimaging and Clinical Features of a Newly Recognized Condition. Journal of Child Neurology, 12(6), 365-368. doi: 10.1177/088307389701200605en_US
dc.identifier.urihttps://hdl.handle.net/11244/25145
dc.description.abstractOther than hamartomatous enlargement of the cerebellum as in Lhermitte-Duclos syndrome, diffuse enlargement of the cerebellum is not clearly described. We report four patients (ages 9 months to 2 years) with diffusely enlarged cerebelli as identified by measurement of the cerebellum and comparison to age appropriate normal values. The cerebellar measurements were determined in absolute numbers and expressed as ratios of cerebellum to whole brain and supratentorial brain. The clinical features of these four children (3 boys, 1 girl) consistently include global developmental delay, tone abnormalities, preserved reflexes, delayed or abnormal maturation of the visual system (oculomotor apraxia), and deficient or delayed myelination of cerebral white matter. The etiology of the macrocerebellum is unknown but we propose that the cerebellum is responding to the elaboration of growth factors intended to augment the slow development of cerebral structures. Regardless of the etiology, the finding of a macrocerebellum appears to allow the clinician to predict the clinical features of the patient and probably represents a marker for disturbed cerebral development. (J Child Neurol 1997;12:365-368).en_US
dc.language.isoen_USen_US
dc.publisherJournal of Child Neurology
dc.titleMacrocerebellum: Neuroimaging and Clinical Features of a Newly Recognized Conditionen_US
dc.typeResearch Articleen_US
dc.description.peerreviewYesen_US
dc.description.peerreviewnoteshttps://us.sagepub.com/en-us/nam/manuscript-submission-guidelinesen_US
dc.identifier.doi10.1177/088307389701200605en_US
dc.rights.requestablefalseen_US


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