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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997
See this aricle in Pubmed

Article Abstract
Machado-Joseph disease(MJD)is an autosomal dominant neurodegenerative disorder associated with the expansion of a(CAG)n array in the MJD1 gene. We analyzed the sizes of the(CAG)n array using DNA samples from 61 members of four Chinese MJD families and 18 Chinese normal control subjects and confirmed that the(CAG)n array in 15 MJD chromosomes was expanded to 72-86 repeat units.There were no subjects with(CAG)n array sizes intermediate between those of normal and MJD affected groups.Meanwhile,we found a significant negative correlation between the age of onset of symptoms and (CAG)n array size.The largest(CAG)n array of 86 repeat units was in the youngest patient,whose age of onset was 5 years.The intergenerational increase in number or CAG repeat units was associated with the clinical phenomenon of anticipation.
 
Related Tags
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CAG repeats
chromosome 14
degenerative diseases of CNS
genetic neurologic disorders
molecular genetics
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
trinucleotide repeats

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