Article
[Current perspectives in the treatment of Huntington's chorea].
Neurologia i neurochirurgia polska - 1 Jan 2000
Kuran Włodzimierz
Abstract excerpt
Huntington's chorea (HD) is a degenerative condition of the central nervous system of genetic origin, inherited as an autosomal dominant trait. The mechanism of the genetic defect is already known, it is a dynamic mutation in the ITI5 gene situated on chromosome 4 p 16.3 coding the protein huntington. The disease is progressive and leading to lethal outcome and effective treatment is unknown. Methods of treatment...
Topics
- Chromosomes, Human, Pair 4
- Diagnosis, Differential
- Genetic Testing
- Humans
- Huntington Disease
- Mutation
- Nerve Degeneration
