Table_2_Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17.XLSX
Suran Nethisinghe
Wei N. Lim
Heather Ging
Anna Zeitlberger
Rosella Abeti
Sally Pemble
Mary G. Sweeney
Robyn Labrum
Charisse Cervera
Henry Houlden
Elisabeth Rosser
Patricia Limousin
Angus Kennedy
Michael P. Lunn
Kailash P. Bhatia
Nicholas W. Wood
John Hardy
James M. Polke
Liana Veneziano
Alfredo Brusco
Mary B. Davis
Paola Giunti
10.3389/fncel.2018.00429.s004
https://frontiersin.figshare.com/articles/dataset/Table_2_Complexity_of_the_Genetics_and_Clinical_Presentation_of_Spinocerebellar_Ataxia_17_XLSX/7377074
<p>Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused by a CAG repeat expansion in the TATA-box binding protein gene (TBP). The disease has a varied age at onset and clinical presentation. It is distinct from other SCAs for its association with dementia, psychiatric symptoms, and some patients presenting with chorea. For this reason, it is also called Huntington’s disease-like 4 (HDL-4). Here we examine the distribution of SCA17 allele repeat sizes in a United Kingdom-based cohort with ataxia and find that fully penetrant pathogenic alleles are very rare (5 in 1,316 chromosomes; 0.38%). Phenotype-genotype correlation was performed on 30 individuals and the repeat structure of their TBP genes was examined. We found a negative linear correlation between total CAG repeat length and age at disease onset and, unlike SCA1, there was no correlation between the longest contiguous CAG tract and age at disease onset. We were unable to identify any particular phenotypic trait that segregated with particular CAG/CAA repeat tract structures or repeat lengths. One individual within the cohort was homozygous for variable penetrance range SCA17 alleles. This patient had a similar age at onset to heterozygotes with the same repeat sizes, but also presented with a rapidly progressive dementia. A pair of monozygotic twins within the cohort presented 3 years apart with the sibling with the earlier onset having a more severe phenotype with dementia and chorea in addition to the ataxia observed in their twin. This appears to be a case of variable expressivity, possibly influenced by other environmental or epigenetic factors. Finally, there was an asymptomatic father with a severely affected child with an age at onset in their twenties. Despite this, they share the same expanded allele repeat sizes and sequences, which would suggest that there is marked difference in the penetrance of this 51-repeat allele. We therefore propose that the variable penetrance range extend from 48 repeats to incorporate this allele. This study shows that there is variability in the presentation and penetrance of the SCA17 phenotype and highlights the complexity of this disorder.</p>
2018-11-23 04:13:06
PolyQ
ataxia
CAG repeat expansions
SCA17
neurodegeneration
genetic counseling