Literature DB >> 8606660

Haemochromatosis--a clinical update.

M J Burt1, D K George, L W Powell.   

Abstract

Haemochromatosis is now known to be a common genetic disorder, with a carrier rate of about 1 in 10 in populations of Northern European origin. With early diagnosis and treatment, life expectancy is normal, yet it remains underdiagnosed.

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Year:  1996        PMID: 8606660

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


  2 in total

1.  Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemia.

Authors:  Hyun Jin Kim; Yoon-Myung Kim; Eungu Kang; Beom Hee Lee; Jin-Ho Choi; Han-Wook Yoo
Journal:  Ann Pediatr Endocrinol Metab       Date:  2017-03-31

2.  Hypoparathyroidism and subclinical hypothyroidism with secondary hemochromatosis.

Authors:  Hyung Ki Jeong; Joon Hwan An; Hyoung Sang Kim; Eun Ae Cho; Min Gui Han; Jung Sik Moon; Hee Kyung Kim; Ho-Cheol Kang
Journal:  Endocrinol Metab (Seoul)       Date:  2014-03-14
  2 in total

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