S. Claes et al., CORRELATIONS BETWEEN TRIPLET REPEAT EXPANSION AND CLINICAL-FEATURES IN HUNTINGTONS-DISEASE, Archives of neurology, 52(8), 1995, pp. 749-753
Objective: To investigate possible correlations between the length of
the (GAG), trinucleotide repeat in Huntington's disease gene IT15 and
clinical features (age at onset, symptoms at onset, and mode of progre
ssion) in Huntington's disease. Design: In 59 patients with Huntington
's disease, the expansion of the (GAG), trinucleotide repeat was deter
mined and clinical data were obtained retrospectively. Setting: The Ce
nter for Human Genetics, affiliated with a university hospital.Patient
s: All patients belonged to an initial group of 248 individuals tested
in an indirect predictive testing procedure. Results: A good correlat
ion was found between the expansion of the (GAG), trinucleotide repeat
and the age at onset (r=-.71). No correlation was found between the r
epeat length of the normal allele and the age at onset. No correlation
s were found between repeat expansion and other clinical features, suc
h as the nature of the symptoms at onset (neurologic, psychiatric/cogn
itive, or both) and the mode of progression. Conclusion: Factors that
determine the nature of symptoms at onset and the mode of progression
of Huntington's disease seem to be operating independently of the (GAG
), trinucleotide repeat in gene IT15.