Literature DB >> 15732233

Thyroid function in haemochromatosis.

M S Murphy1, C H Walsh.   

Abstract

BACKGROUND: In hereditary haemochromatosis (HH), the thyroid gland is the site of substantial iron deposition. However, there have been relatively few reported cases of thyroid dysfunction in HH. AIM: To evaluate the prevalence of thyroid disorders in a large group of patients with HH.
METHODS: A variety of endocrine investigations were undertaken including thyroid function tests and thyroid antibody studies.
RESULTS: A total of 154 consecutive patients (123 male, 31 female) were studied. One case of primary hypothyroidism was identified, giving a prevalence of 0.6%. Subclinical hypothyroidism was identified in two females, giving a prevalence of 1.3%. Iatrogenic hypothyroidism was identified in two other cases. No case of hyperthyroidism was identified.
CONCLUSION: Thyroid dysfunction is an uncommon occurrence in patients with HH.

Entities:  

Mesh:

Year:  2004        PMID: 15732233     DOI: 10.1007/bf02914520

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  19 in total

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  5 in total

Review 1.  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

2.  Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study.

Authors:  James C Barton; Catherine Leiendecker-Foster; David M Reboussin; Paul C Adams; Ronald T Acton; John H Eckfeldt
Journal:  Thyroid       Date:  2008-08       Impact factor: 6.568

3.  All that is hypogonadal in haemochromatosis is not due to iron deposition.

Authors:  E P O'Sullivan; J H McDermott; C Howel Walsh
Journal:  Ir J Med Sci       Date:  2007-03       Impact factor: 1.568

4.  Longitudinal study on thyroid function in patients with thalassemia major: High incidence of central hypothyroidism by 18 years.

Authors:  Ashraf T Soliman; Fawzia Al Yafei; Lolwa Al-Naimi; Noora Almarri; Aml Sabt; Mohamed Yassin; Vincenzo De Sanctis
Journal:  Indian J Endocrinol Metab       Date:  2013-11

5.  Autoimmune Conditions in 235 Hemochromatosis Probands with HFE C282Y Homozygosity and Their First-Degree Relatives.

Authors:  James C Barton; J Clayborn Barton
Journal:  J Immunol Res       Date:  2015-10-04       Impact factor: 4.818

  5 in total

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