Journal article
White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism
DZ Loesch, K Kotschet, N Trost, CM Greco, G Kinsella, HR Slater, A Venn, M Horne
American Journal of Medical Genetics Part B Neuropsychiatric Genetics | WILEY-BLACKWELL | Published : 2011
DOI: 10.1002/ajmg.b.31189
Abstract
Examples of white matter hyperintensities (wmh) on magnetic resonance images in a basis pontis are presented in two male carriers, each of whom carry a small CGG expansion fragile X mental retardation (FMR1) allele. One carried a premutation (PM) allele of 85 CGG repeats and the other, a gray zone (GZ) allele of 47 repeats. Both were originally diagnosed with idiopathic Parkinson's disease (iPD). Similar changes are also shown in one PM carrier of 99 repeats affected with mild tremor and imbalance, who was ascertained through a fragile X syndrome family. These examples draw attention to the occurrence of wmh in a basis pontis in the carriers of small CGG expansions presenting with tremor and..
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Awarded by National Institute of Child Health and Human Development
Funding Acknowledgements
This study was supported by the National Institutes of Child Health and Human Development Grant HD 36071 and NHMRC project grant no. 330400 to Dr. D. Z. Loesch.