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Adrenomyeloneuropathy Presenting With Adrenal Insufficiency

Adrenomyeloneuropathy (AMN), one of the variants of X-linked adrenoleukodystrophy (ALD), is inherited peroxisomal disorder associated with the accumulation of very long chain fatty acids (VLCFA). AMN is characterized primarily by involvements of long ascending and descending tracts of the spinal cor...

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Autores principales: Park, Hee Dong, Park, Sang Jun, Choi, Yong Min, Kang, Jin Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Academy of Rehabilitation Medicine 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764352/
https://www.ncbi.nlm.nih.gov/pubmed/24020038
http://dx.doi.org/10.5535/arm.2013.37.4.563
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author Park, Hee Dong
Park, Sang Jun
Choi, Yong Min
Kang, Jin Ho
author_facet Park, Hee Dong
Park, Sang Jun
Choi, Yong Min
Kang, Jin Ho
author_sort Park, Hee Dong
collection PubMed
description Adrenomyeloneuropathy (AMN), one of the variants of X-linked adrenoleukodystrophy (ALD), is inherited peroxisomal disorder associated with the accumulation of very long chain fatty acids (VLCFA). AMN is characterized primarily by involvements of long ascending and descending tracts of the spinal cord and peripheral neuropathy, which leads to spastic paraparesis and urinary and erectile dysfunction. We experienced the AMN case of a 33-year-old man presenting bilateral progressive spastic paraparesis, impotence and urge incontinence with primary adrenal failures, as confirmed by increased serum of VLCFA concentrations. Considering that somatosensory evoked potentials in posterior tibial nerve was the only abnormal finding in electrophysiologic findings when compared with the severe spastic gait pattern shown, it is necessary to follow up with electrophysiologic studies.
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spelling pubmed-37643522013-09-09 Adrenomyeloneuropathy Presenting With Adrenal Insufficiency Park, Hee Dong Park, Sang Jun Choi, Yong Min Kang, Jin Ho Ann Rehabil Med Case Report Adrenomyeloneuropathy (AMN), one of the variants of X-linked adrenoleukodystrophy (ALD), is inherited peroxisomal disorder associated with the accumulation of very long chain fatty acids (VLCFA). AMN is characterized primarily by involvements of long ascending and descending tracts of the spinal cord and peripheral neuropathy, which leads to spastic paraparesis and urinary and erectile dysfunction. We experienced the AMN case of a 33-year-old man presenting bilateral progressive spastic paraparesis, impotence and urge incontinence with primary adrenal failures, as confirmed by increased serum of VLCFA concentrations. Considering that somatosensory evoked potentials in posterior tibial nerve was the only abnormal finding in electrophysiologic findings when compared with the severe spastic gait pattern shown, it is necessary to follow up with electrophysiologic studies. Korean Academy of Rehabilitation Medicine 2013-08 2013-08-26 /pmc/articles/PMC3764352/ /pubmed/24020038 http://dx.doi.org/10.5535/arm.2013.37.4.563 Text en Copyright © 2013 by Korean Academy of Rehabilitation Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Park, Hee Dong
Park, Sang Jun
Choi, Yong Min
Kang, Jin Ho
Adrenomyeloneuropathy Presenting With Adrenal Insufficiency
title Adrenomyeloneuropathy Presenting With Adrenal Insufficiency
title_full Adrenomyeloneuropathy Presenting With Adrenal Insufficiency
title_fullStr Adrenomyeloneuropathy Presenting With Adrenal Insufficiency
title_full_unstemmed Adrenomyeloneuropathy Presenting With Adrenal Insufficiency
title_short Adrenomyeloneuropathy Presenting With Adrenal Insufficiency
title_sort adrenomyeloneuropathy presenting with adrenal insufficiency
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764352/
https://www.ncbi.nlm.nih.gov/pubmed/24020038
http://dx.doi.org/10.5535/arm.2013.37.4.563
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