Literature DB >> 9553847

Determinants of onset age in Friedreich's ataxia.

G De Michele1, A Filla, C Criscuolo, V Scarano, F Cavalcanti, L Pianese, A Monticelli, S Cocozza.   

Abstract

We studied the factors that might influence onset age in Friedreich's ataxia in 41 cases (20 male, 21 female) homozygous for GAA expansion on the first intron of X25 gene. Patients came from 18 multiplex families (13 couples, 5 triplets). Mean age (SD) was 18.1 (8.9) years and did not differ by gender. Onset age and the sizes of the smaller (GAA1) and the larger (GAA2) allele in each pair showed high intrafamily correlation. We found an inverse correlation between age at onset and GAA1 size, but not between age at onset and GAA2 size. Stepwise multiple regression of onset age on GAA1 size, sibling onset age, and GAA2 size showed that GAA1 accounts for 73% of onset age variance, and sibling onset age for an additional 13%. The study demonstrates that, in addition to GAA expansion size, other environmental or genetic familial factors influence disease expression.

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Year:  1998        PMID: 9553847     DOI: 10.1007/s004150050198

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  14 in total

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7.  Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features.

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9.  The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.

Authors:  A Filla; G De Michele; F Cavalcanti; L Pianese; A Monticelli; G Campanella; S Cocozza
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

10.  Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.

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7.  A universal mechanism ties genotype to phenotype in trinucleotide diseases.

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Review 8.  Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington's Disease.

Authors:  Xiaonan Zhao; Daman Kumari; Carson J Miller; Geum-Yi Kim; Bruce Hayward; Antonia G Vitalo; Ricardo Mouro Pinto; Karen Usdin
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