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Twenty years of dysuria in a patient with Addison’s disease: a case report

X-linked adrenoleukodystrophy is an X-linked recessive disorder affecting approximately 1 in 21,000 males, and is estimated to be the cause of adrenal insufficiency in approximately 35% of patients with idiopathic Addison’s disease. The disease is caused by defective beta-oxidation of fatty acids in...

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Autores principales: Nanci, Gabriella N, Collier, Millard J, Rose, Sheldon H
Formato: Texto
Lenguaje:English
Publicado: Cases Network Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740147/
https://www.ncbi.nlm.nih.gov/pubmed/19830040
http://dx.doi.org/10.4076/1757-1626-2-7995
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author Nanci, Gabriella N
Collier, Millard J
Rose, Sheldon H
author_facet Nanci, Gabriella N
Collier, Millard J
Rose, Sheldon H
author_sort Nanci, Gabriella N
collection PubMed
description X-linked adrenoleukodystrophy is an X-linked recessive disorder affecting approximately 1 in 21,000 males, and is estimated to be the cause of adrenal insufficiency in approximately 35% of patients with idiopathic Addison’s disease. The disease is caused by defective beta-oxidation of fatty acids in peroxisomes that leads to elevated serum concentrations of very-long-chain saturated fatty acids. The accumulation causes a primary adrenal insufficiency and progressive neurological dysfunction. This article presents a case of X-linked adrenoleukodystrophy in its milder form, adrenomyeloneuropathy.
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spelling pubmed-27401472009-10-14 Twenty years of dysuria in a patient with Addison’s disease: a case report Nanci, Gabriella N Collier, Millard J Rose, Sheldon H Cases J Case report X-linked adrenoleukodystrophy is an X-linked recessive disorder affecting approximately 1 in 21,000 males, and is estimated to be the cause of adrenal insufficiency in approximately 35% of patients with idiopathic Addison’s disease. The disease is caused by defective beta-oxidation of fatty acids in peroxisomes that leads to elevated serum concentrations of very-long-chain saturated fatty acids. The accumulation causes a primary adrenal insufficiency and progressive neurological dysfunction. This article presents a case of X-linked adrenoleukodystrophy in its milder form, adrenomyeloneuropathy. Cases Network Ltd 2009-06-15 /pmc/articles/PMC2740147/ /pubmed/19830040 http://dx.doi.org/10.4076/1757-1626-2-7995 Text en © 2009 Nanci et al.; licensee Cases Network Ltd. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case report
Nanci, Gabriella N
Collier, Millard J
Rose, Sheldon H
Twenty years of dysuria in a patient with Addison’s disease: a case report
title Twenty years of dysuria in a patient with Addison’s disease: a case report
title_full Twenty years of dysuria in a patient with Addison’s disease: a case report
title_fullStr Twenty years of dysuria in a patient with Addison’s disease: a case report
title_full_unstemmed Twenty years of dysuria in a patient with Addison’s disease: a case report
title_short Twenty years of dysuria in a patient with Addison’s disease: a case report
title_sort twenty years of dysuria in a patient with addison’s disease: a case report
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740147/
https://www.ncbi.nlm.nih.gov/pubmed/19830040
http://dx.doi.org/10.4076/1757-1626-2-7995
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