Literature DB >> 23337002

A magnetic resonance imaging study of cerebellar volume in tuberous sclerosis complex.

Neil I Weisenfeld1, Jurriaan M Peters, Peter T Tsai, Sanjay P Prabhu, Kira A Dies, Mustafa Sahin, Simon K Warfield.   

Abstract

The cerebellum plays an important role in motor learning and cognition, and structural cerebellar abnormalities have been associated with cognitive impairment. In tuberous sclerosis complex, neurologic outcome is highly variable, and no consistent imaging or pathologic determinant of cognition has been firmly established. The cerebellum calls for specific attention because mouse models of tuberous sclerosis complex have demonstrated a loss of cerebellar Purkinje cells, and cases of human histologic data have demonstrated a similar loss in patients. We hypothesized that there might be a common cerebellar finding in tuberous sclerosis complex that could be measured as morphometric changes with magnetic resonance imaging. Using a robust, automated image analysis procedure, we studied 36 patients with tuberous sclerosis complex and age-matched control subjects and observed significant volume loss among patients in the cerebellar cortices and vermis. Furthermore, this effect was strongest in a subgroup of 19 patients with a known, pathogenic mutation of the tuberous sclerosis 2 gene and impacted all cerebellar structures. We conclude that patients with tuberous sclerosis complex exhibit volume loss in the cerebellum, and this loss is larger and more widespread in patients with a tuberous sclerosis 2 mutation.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23337002      PMCID: PMC3763730          DOI: 10.1016/j.pediatrneurol.2012.10.011

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  46 in total

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4.  Loss of the tuberous sclerosis complex protein tuberin causes Purkinje cell degeneration.

Authors:  R Michelle Reith; Sharon Way; James McKenna; Katherine Haines; Michael J Gambello
Journal:  Neurobiol Dis       Date:  2011-03-17       Impact factor: 5.996

5.  Expression of the tuberous sclerosis complex gene products, hamartin and tuberin, in central nervous system tissues.

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Review 9.  Mechanisms of neurocognitive dysfunction and therapeutic considerations in tuberous sclerosis complex.

Authors:  Peter Tsai; Mustafa Sahin
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Authors:  Ling-Hui Zeng; Nicholas R Rensing; Bo Zhang; David H Gutmann; Michael J Gambello; Michael Wong
Journal:  Hum Mol Genet       Date:  2010-11-09       Impact factor: 6.150

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  12 in total

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Review 3.  Imaging genetics in neurodevelopmental psychopathology.

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4.  Diffusion tensor imaging and related techniques in tuberous sclerosis complex: review and future directions.

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Review 5.  Lessons learned from studying syndromic autism spectrum disorders.

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7.  Cerebellar volume as an imaging marker of development in infants with tuberous sclerosis complex.

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Review 8.  The role of cerebellar circuitry alterations in the pathophysiology of autism spectrum disorders.

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Review 9.  Autism spectrum disorders and neuropathology of the cerebellum.

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10.  Loss of Tsc1 in cerebellar Purkinje cells induces transcriptional and translation changes in FMRP target transcripts.

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