Literature DB >> 758139

Idiopathic hemochromatosis in a young female. A case study and review of the syndrome in young people.

J M Lamon, S P Marynick, R Roseblatt, S Donnelly.   

Abstract

Idiopathic hemochromatosis (iH) is typically a disease of older males. The case presented here describes a 26-yr-old woman with problems presenting heart failure, insulin-dependent diabetes, hepatomegaly, and secondary amenorrhea. The diagnosis was established by serum iron and transferrin saturation measurements, liver biopsy, and bone marrow examination for iron. Twenty grams of iron were removed by phlebotomy over 30 mo, and the patient's symptoms improved. A review of the literature pertinent to people with symptomatic onset of IH before age 30 yr revealed 52 young people in addition to this case. In contrast to IH patients older than 30, there was an almost equal ratio between the sexes, a greater frequency of cardiomyopathy and hypogonadism, and a lower frequency of diabetes mellitus and hepatic involvement. An autosomal recessive mode of inheritance appears to be most likely in this young group.

Entities:  

Mesh:

Year:  1979        PMID: 758139

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  16 in total

Review 1.  Osteoporosis in HFE2 juvenile hemochromatosis. A case report and review of the literature.

Authors:  Nicholas G Angelopoulos; Anastasia K Goula; George Papanikolaou; George Tolis
Journal:  Osteoporos Int       Date:  2005-07-05       Impact factor: 4.507

2.  Hepatobiliary Quiz Answers-17 (2016).

Authors:  Sahaj Rathi; Radha K Dhiman
Journal:  J Clin Exp Hepatol       Date:  2016-05-04

3.  Multiple organ dysfunction in a 33-year-old woman due to hereditary hemochromatosis.

Authors:  Y Niihara; D W Brouwer; K A Cantos
Journal:  West J Med       Date:  1995-04

4.  A non-transferrin-bound serum iron in idiopathic hemochromatosis.

Authors:  R G Batey; P Lai Chung Fong; S Shamir; S Sherlock
Journal:  Dig Dis Sci       Date:  1980-05       Impact factor: 3.199

5.  Atypical haemochromatosis: phenotypic spectrum and beta2-microglobulin candidate gene analysis.

Authors:  A P Walker; D F Wallace; J Partridge; A B Bomford; J S Dooley
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

Review 6.  Endocrine dysfunction in hereditary hemochromatosis.

Authors:  C Pelusi; D I Gasparini; N Bianchi; R Pasquali
Journal:  J Endocrinol Invest       Date:  2016-03-07       Impact factor: 4.256

7.  Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis.

Authors:  S Pinson; J Yaouanq; A M Jouanolle; B Turlin; H Plauchu
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

8.  Non-HFE hemochromatosis.

Authors:  Paulo Caleb Júnior de Lima Santos; Carla Luana Dinardo; Rodolfo Delfini Cançado; Isolmar Tadeu Schettert; José Eduardo Krieger; Alexandre Costa Pereira
Journal:  Rev Bras Hematol Hemoter       Date:  2012

9.  Juvenile idiopathic haemochromatosis: a life-threatening disorder presenting as hypogonadotropic hypogonadism.

Authors:  M Cazzola; E Ascari; G Barosi; G Claudiani; M Daccó; J P Kaltwasser; N Panaiotopoulos; K P Schalk; E E Werner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

Review 10.  Non-HFE haemochromatosis.

Authors:  Daniel-F Wallace; V-Nathan Subramaniam
Journal:  World J Gastroenterol       Date:  2007-09-21       Impact factor: 5.742

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.