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Two Cases of Sporadic Juvenile Parkinson's Disease Caused by Homozygous Deletion of Parkin Gene Hiroshi Ujike 1 , Mitsutoshi Yamamoto 2 , Koji Yamaguchi 3 , Akihiro Kanzaki 4 , Manabu Takagi 1 , Shigetoshi Kuroda 1 1Department of Neuropsychiatry, Okayama University Medical School 2Department of Neurology, Kagawa Central Hospital 3Department of Neurology, Midori Hospital 4Department of Neurology, Tottori Municipal Hospital Keyword: parkin gene , delection , juvenile parkinsonism , sporadic case pp.1061-1064
Published Date 1999/12/1
DOI https://doi.org/10.11477/mf.1406901531
  • Abstract
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Parkin gene, which is one of the causes of familial Parkinson's disease, was cloned in 1998, and it was found that mutations of this gene induces familial Parkinson's disease of autosomal recessive form (AR-JP). Clinical studies have revealed that almost cases of AR-P are consanguineous or hereditary. However, AR-P may also be caused by marriage between two carriers. We therefore investigated the existence of a homozygous deletion in the parkin gene in 10 patients with juvenile Parkinson's disease with the onset of age younger than 40 years without consanguinity or he-redity.


Copyright © 1999, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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