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

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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University of Melbourne Researchers