A Case of Hereditary Hemochromatosis (HH) with Left Ventricular Dysfunction-Reference-Cited by-同舟云学术

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A Case of Hereditary Hemochromatosis (HH) with Left Ventricular Dysfunction

Published:2012 Issue:4 Volume:101 Page:1069-1071
ISSN:0021-5384
Container-title:Nihon Naika Gakkai Zasshi
language:en
Short-container-title:J. Jpn. Soc. Intern. Med

Author:

Iwayama Kosaka¹,Sugita Junichi¹,Fukushima Kazuyuki¹,Ikenouchi Hiroshi¹,Suzuki Kenshi²,Maeda Takashi³,Tomoyasu Shigeru³

Affiliation:

1. Department of Cardiology, Japanese Red Cross Medical Center

2. Department of Hematology, Japanese Red Cross Medical Center

3. Department of Hematology, Showa University

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/naika/101/4/101_1069/_pdf

Reference6 articles.

1. 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.

2. 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. 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. 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.

5. 5) Hayashi H, et al: Genetic background of Japanese patients with adult-onset storage diseases in the liver. Hepatology Research 37: 777-783, 2007.

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