JPH3 repeat expansions cause a progressive akinetic-rigid syndrome with severe dementia and putaminal rim in a five-generation African-American family

Susanne A. Schneider, Kate E. Marshall, Jianfeng Xiao, Mark S. LeDoux*

*Korrespondierende/r Autor/-in für diese Arbeit
11 Zitate (Scopus)

Abstract

We report the clinical, neuropsychological, genetic, and radiological features of a large five-generation African-American kindred from the southern USA presenting with a progressive akinetic-rigid syndrome and severe dementia, but clinically insignificant chorea, due to mutations in junctophillin 3 (JPH3). Overt disease onset was in the mid-20s to late 30s with cognitive decline, REM sleep disturbance, or psychiatric features, followed by development of a levodopaunresponsive akinetic-rigid motor syndrome. Dystonia and myoclonus were present in some subjects. A bedridden, non-verbal severely akinetic-rigid state developed within 10 to 15 years after onset. CTG repeat expansions ranged from 47 to 53. Imaging revealed generalized cerebral atrophy with severe striatal involvement and putaminal rim hyperintensity. Analysis of our kindred indicates that JPH3 mutations should be considered in the differential diagnosis of early-onset dementia and hypokinetic-rigid syndromes in individuals of African descent.Moreover, choreamay not be overtly manifest at presentation or during significant parts of the disease course.

OriginalspracheEnglisch
ZeitschriftNeurogenetics
Jahrgang13
Ausgabenummer2
Seiten (von - bis)133-140
Seitenumfang8
ISSN1364-6745
DOIs
PublikationsstatusVeröffentlicht - 01.05.2012

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