Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease
β Scribed by J. Benitez; E. Fernandez; P. Garcia Ruiz; M. Robledo; C. Ramos; J. Yebenes
- Publisher
- Springer
- Year
- 1994
- Tongue
- English
- Weight
- 182 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0340-6717
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β¦ Synopsis
Huntington's disease (HD) is a neurodegenerative and hereditary disease characterized by progressive movement disorders and mental and behavioral abnormalities. The HD gene is an expanding and unstable trinucleotide repeat (CAG repeat sequences). We studied 77 individuals from 38 families with HD in an attempt to obtain information for genetic counselling and differential diagnosis. Our results indicate that individuals with more than 40 repeats will be affected by the disease, whereas those with fewer than 30 will be healthy. There can be some overlap between 30 and 40 repeats, and one should be careful when interpreting these results.
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## Communicated by Christine Van Broeckhoven Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized clinically by progressive motor impairment, cognitive decline, and emotional deterioration. The disease is caused by the abnormal expansion of a CAG trinucleotide
## Abstract We describe and present a video of a patient with maternally inherited juvenile Huntington's disease (HD) caused by a very large (108βrepeat) expansion. Maternally transmitted very large trinucleotide repeats (>100) are extremely rare in juvenile HD and may represent instability during