Journal of pediatric and neonatal individualized medicine jpnim. Huntingtondisease hd is a degenerative dysfunction of hereditary origin. Huntingtin is the abnormal protein produced by the repeat of the cag triplet. Files are available under licenses specified on their description page. Huntington s disease uncountable medicine, neurology a hereditary disorder of the basal ganglia that leads to progressive loss of motor coordination. Huntington disease has severe implications, not only in the quality of life of the patient, but also in the family and social set ting. Huntington disease is an autosomal dominantly transmitted disorder. Therapy of chorea associated with huntingtons disease. Pdf huntingtons disease hd has been recognized as one of the three. All structured data from the file and property namespaces is available under the creative commons cc0 license. It is caused by a mutation in it15 gene on chromosome 4p16. Targeted disruption of the huntingtons disease gene results in embryonic. You can access the page containing the full pdf article just by clicking on the full text. Huntington disease and related disorders, eye degenerative disease.
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