Hemochromatosis Type I. Pathogenia and Diagnosis

<p>Hemochromatosis type 1 is a genetic disease characterized by high iron absorption at the intestinal crypts due to an alteration in their metabolism, causing progressive accumulation in a variety of organs. It should be diagnosed in pre-clinical stages through genetic and biochemical tests;...

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Main Author: Ismael Aramís Cervera García
Format: Article
Language:Spanish
Published: Centro Provincial de Información de Ciencias Médicas. Cienfuegos 2012-05-01
Series:Medisur
Subjects:
Online Access:http://medisur.sld.cu/index.php/medisur/article/view/1727
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author Ismael Aramís Cervera García
author_facet Ismael Aramís Cervera García
author_sort Ismael Aramís Cervera García
collection DOAJ
description <p>Hemochromatosis type 1 is a genetic disease characterized by high iron absorption at the intestinal crypts due to an alteration in their metabolism, causing progressive accumulation in a variety of organs. It should be diagnosed in pre-clinical stages through genetic and biochemical tests; some patients are diagnosed late, that is after symptoms appear which is considered to be a failure given that diagnosis during asymptomatic phase could prevent serious organs complications of the disease. Its incidence in Cuba has not been reported and, although molecular diagnostics have just been introduced in our context, it continues to be performed from patient's clinical characteristics and quantification of serum iron and ferritin, so that asymptomatic patients or carriers can not be identified yet. For all these reasons this review was conducted so that doctors know more about this condition and the means available for an appropriate diagnosis.</p>
format Article
id doaj-art-88384219791e47fa9bcf78a421155386
institution Kabale University
issn 1727-897X
language Spanish
publishDate 2012-05-01
publisher Centro Provincial de Información de Ciencias Médicas. Cienfuegos
record_format Article
series Medisur
spelling doaj-art-88384219791e47fa9bcf78a4211553862025-01-30T21:28:45ZspaCentro Provincial de Información de Ciencias Médicas. CienfuegosMedisur1727-897X2012-05-01102128135858Hemochromatosis Type I. Pathogenia and DiagnosisIsmael Aramís Cervera García0Centro Nacional de Genética Médica.Cuba.<p>Hemochromatosis type 1 is a genetic disease characterized by high iron absorption at the intestinal crypts due to an alteration in their metabolism, causing progressive accumulation in a variety of organs. It should be diagnosed in pre-clinical stages through genetic and biochemical tests; some patients are diagnosed late, that is after symptoms appear which is considered to be a failure given that diagnosis during asymptomatic phase could prevent serious organs complications of the disease. Its incidence in Cuba has not been reported and, although molecular diagnostics have just been introduced in our context, it continues to be performed from patient's clinical characteristics and quantification of serum iron and ferritin, so that asymptomatic patients or carriers can not be identified yet. For all these reasons this review was conducted so that doctors know more about this condition and the means available for an appropriate diagnosis.</p>http://medisur.sld.cu/index.php/medisur/article/view/1727hemocromatosisdiagnóstico
spellingShingle Ismael Aramís Cervera García
Hemochromatosis Type I. Pathogenia and Diagnosis
Medisur
hemocromatosis
diagnóstico
title Hemochromatosis Type I. Pathogenia and Diagnosis
title_full Hemochromatosis Type I. Pathogenia and Diagnosis
title_fullStr Hemochromatosis Type I. Pathogenia and Diagnosis
title_full_unstemmed Hemochromatosis Type I. Pathogenia and Diagnosis
title_short Hemochromatosis Type I. Pathogenia and Diagnosis
title_sort hemochromatosis type i pathogenia and diagnosis
topic hemocromatosis
diagnóstico
url http://medisur.sld.cu/index.php/medisur/article/view/1727
work_keys_str_mv AT ismaelaramiscerveragarcia hemochromatosistypeipathogeniaanddiagnosis