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A Japanese case of idiopathic hemochromatosis with analysis of HFE gene mutations and a review of literature on HLA phenotypes in the Japanese cases
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- FUJITA Jun
- Department of Internal Medicine, Nippon Kokan Hospital
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- INAGAKI Yasutaka
- Department of Internal Medicine, Nippon Kokan Hospital
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- YONEI Yoshikazu
- Department of Internal Medicine, Nippon Kokan Hospital
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- OTSUKA Seiji
- Department of Internal Medicine, Nippon Kokan Hospital
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- NAKAZAWA Atsushi
- Department of Internal Medicine, Nippon Kokan Hospital
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- TSUKADA Nobuhiro
- Department of Internal Medicine, Nippon Kokan Hospital
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- SUZUKI Osamu
- Department of Internal Medicine, Nippon Kokan Hospital
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- KIRYU Yasuyoshi
- Department of Internal Medicine, Nippon Kokan Hospital
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- MIZUNO Yoshio
- Department of Internal Medicine, Nippon Kokan Hospital
Bibliographic Information
- Other Title
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- 日本人特発性ヘモクロマトーシスの１例 ＨＦＥ遺伝子変異の検索と本邦報告例ＨＬＡの文献的検討
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Description
症例は45歳男性の特発性ヘモクロマトーシス．皮膚色素沈着，糖尿病，肝線維化，下垂体性腺機能低下を呈しHLAはA11，A31(19)，B46，B60(40)，Cw1，Cw7でHFE遺伝子変異(C282Y，H63D)を認めなかった．更にHLAの記載のある本邦報告25例につき文献的に検討した結果欧米症例で高率なHLAA3，B7，B14の頻度は本邦症例では極めてまれであり人種差が認められた．
Journal
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- Nippon Shokakibyo Gakkai Zasshi
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Nippon Shokakibyo Gakkai Zasshi 97 (4), 472-477, 2000
The Japanese Society of Gastroenterology
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Details 詳細情報について
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- CRID
- 1390001206396688256
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- NII Article ID
- 10007001947
- 10005558146
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- NII Book ID
- AN00192124
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- COI
- 1:STN:280:DC%2BD3c3lsVSnsA%3D%3D
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- ISSN
- 13497693
- 04466586
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- PubMed
- 10793572
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- Text Lang
- ja
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- Article Type
- journal article
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- Data Source
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- JaLC
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed