Literature DB >> 7353757

Idiopathic hemochromatosis: a study of biochemical expression in 247 heterozygous members of 63 families: evidence for a single major HLA-linked gene.

M Simon, R Fauchet, J P Hespel, C Beaumont, P Brissot, B Hery, Y Hita De Nercy, B Genetet, M Bourel.   

Abstract

The hypothesis has been advanced that the two genes on chromosome 6 determining idiopathic hemochromatosis are not identical alleles and therefore that the disease is not recessively inherited, but rather that two different genes are involved. A study of 63 families points to: (a) the rarity with which a single hemochromatosis gene finds biochemical expression (in only 1 of 5 cases), as revealed through determinations of serum iron, serum ferritin and the desferrioxamine test; (b) no difference in HLA-antigen marking between genes with and those without biochemical expression: (c) no difference other than that produced by chance in the biochemical expression of the two genes in families; and (d) the finding in one highly informative family of identical expression of the two genes. It is concluded that idiopathic hemochromatosis is determined by two homologous alleles in accordance with the classical mode of recessive inheritance.

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Year:  1980        PMID: 7353757

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


  8 in total

1.  Articular manifestations of systemic diseases.

Authors:  W G Bensen
Journal:  Can Fam Physician       Date:  1983-11       Impact factor: 3.275

2.  HLA as a marker of the hemochromatosis gene in Sweden.

Authors:  B Ritter; J Säfwenberg; K S Olsson
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

3.  The significance of haemochromatosis gene mutations in the general population: implications for screening.

Authors:  M J Burt; P M George; J D Upton; J A Collett; C M Frampton; T M Chapman; T A Walmsley; B A Chapman
Journal:  Gut       Date:  1998-12       Impact factor: 23.059

4.  Iron and haemochromatosis.

Authors:  M Worwood
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

5.  The use of association data to identify family members at high risk for marker-linked diseases.

Authors:  W J Conte; J I Rotter
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

6.  Increased PiZ gene frequency for alpha 1 antitrypsin in patients with genetic haemochromatosis.

Authors:  A N Elzouki; R Hultcrantz; P Stål; R Befrits; S Eriksson
Journal:  Gut       Date:  1995-06       Impact factor: 23.059

7.  Segregation of genetic hemochromatosis indexed by latent capacity of transferrin.

Authors:  I B Borecki; D C Rao; J Yaouanq; J M Lalouel
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

8.  Idiopathic hemochromotosis and alpha-1-antitrypsin deficiency: coexistence in a family with progressive liver disease in the proband.

Authors:  S Anand; R R Schade; C Bendetti; R Kelly; B S Rabin; J Krause; T E Starzl; S Iwatsuki; D H Van Thiel
Journal:  Hepatology       Date:  1983 Sep-Oct       Impact factor: 17.425

  8 in total

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