左室機能低下を来した遺伝性ヘモクロマトーシスの1例
29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳時にhereditary hemochromatosis(HH)と診断,加療されるも19歳時より自己中断.HHによる心機能障害と考え,心不全の薬物治療に加え除鉄を施行.遺伝子検査にてHemojuvelin(HJV)遺伝子異常によるHHと診断.加療により血清フェリチン,肝機能,心不全症状は改善し外来通院中である....
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Published in | 日本内科学会雑誌 Vol. 101; no. 4; pp. 1069 - 1071 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
一般社団法人 日本内科学会
2012
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Subjects | |
Online Access | Get full text |
ISSN | 0021-5384 1883-2083 |
DOI | 10.2169/naika.101.1069 |
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Abstract | 29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳時にhereditary hemochromatosis(HH)と診断,加療されるも19歳時より自己中断.HHによる心機能障害と考え,心不全の薬物治療に加え除鉄を施行.遺伝子検査にてHemojuvelin(HJV)遺伝子異常によるHHと診断.加療により血清フェリチン,肝機能,心不全症状は改善し外来通院中である. |
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AbstractList | 29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳時にhereditary hemochromatosis(HH)と診断,加療されるも19歳時より自己中断.HHによる心機能障害と考え,心不全の薬物治療に加え除鉄を施行.遺伝子検査にてHemojuvelin(HJV)遺伝子異常によるHHと診断.加療により血清フェリチン,肝機能,心不全症状は改善し外来通院中である. |
Author | 杉田, 純一 鈴木, 憲史 友安, 茂 前田, 崇 岩山, 香坂 池ノ内, 浩 福島, 和之 |
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References | 6) Hayashi H, et al: Genetic Background of Primary Iron Overload Syndromes in Japan. Internal Medicine 45 (20): 1107-1111, 2006. 1) Hachiya M, et al: Hereditary Hemochromatosis Not Associated with Common HFE Gene Mutation in Japanese Siblings. Journal of Pediatric Gastroenterology and Nutrition 32: 501-503, 2001. 5) Hayashi H, et al: Genetic background of Japanese patients with adult-onset storage diseases in the liver. Hepatology Research 37: 777-783, 2007. 2) Koyama C, et al: Three patients with middle-age-onset hemochromatosis caused by novel mutations in the hemojuvelin gene. Journal of Hepatology 43: 740-742, 2005. 3) Nagayoshi Y, et al: A Q312X mutation in the hemojuvelin gene is associated withcardiomyopathy due to juvenile haemochromatosis. European Journal of Heart Failure 10: 1001-1006, 2008. 4) Kaneko Y, et al: Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders. J Gastroenterol 45: 1163-1171, 2010. |
References_xml | – reference: 1) Hachiya M, et al: Hereditary Hemochromatosis Not Associated with Common HFE Gene Mutation in Japanese Siblings. Journal of Pediatric Gastroenterology and Nutrition 32: 501-503, 2001. – reference: 2) Koyama C, et al: Three patients with middle-age-onset hemochromatosis caused by novel mutations in the hemojuvelin gene. Journal of Hepatology 43: 740-742, 2005. – reference: 4) Kaneko Y, et al: Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders. J Gastroenterol 45: 1163-1171, 2010. – reference: 5) Hayashi H, et al: Genetic background of Japanese patients with adult-onset storage diseases in the liver. Hepatology Research 37: 777-783, 2007. – reference: 3) Nagayoshi Y, et al: A Q312X mutation in the hemojuvelin gene is associated withcardiomyopathy due to juvenile haemochromatosis. European Journal of Heart Failure 10: 1001-1006, 2008. – reference: 6) Hayashi H, et al: Genetic Background of Primary Iron Overload Syndromes in Japan. Internal Medicine 45 (20): 1107-1111, 2006. |
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Snippet | 29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳... |
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SubjectTerms | HJV遺伝子 デフェラシロクス 遺伝性ヘモクロマトーシス |
Title | 左室機能低下を来した遺伝性ヘモクロマトーシスの1例 |
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