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Rare variability in adrenoleukodystrophy: a case report

BACKGROUND: X-linked adrenoleukodystrophy is a genetic disorder with diverse clinical phenotypes. Of these phenotypes, the cerebral form usually manifests during early childhood with rapid cognitive and neurological deterioration and is accompanied by extensive white matter involvement. Adrenomyelon...

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Autores principales: Chen, Yanming, Polara, Farhana, Pillai, Anjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022434/
https://www.ncbi.nlm.nih.gov/pubmed/29950168
http://dx.doi.org/10.1186/s13256-018-1722-z
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author Chen, Yanming
Polara, Farhana
Pillai, Anjana
author_facet Chen, Yanming
Polara, Farhana
Pillai, Anjana
author_sort Chen, Yanming
collection PubMed
description BACKGROUND: X-linked adrenoleukodystrophy is a genetic disorder with diverse clinical phenotypes. Of these phenotypes, the cerebral form usually manifests during early childhood with rapid cognitive and neurological deterioration and is accompanied by extensive white matter involvement. Adrenomyeloneuropathy, however, usually affects young adults and has focal symptoms typical of spinal cord and peripheral nerve involvement. CASE PRESENTATION: A 35-year-old African American man with a history of alcohol abuse presented with personality changes and lower extremity weakness. Diffuse demyelination was found on the brain image, and a diagnosis of the cerebral form was made based on the clinical features and genetic test. CONCLUSIONS: We report a rare case of adult-onset cerebral X-linked leukodystrophy with a clinical phenotype of adrenomyeloneuropathy, and the diagnosis was confounded by a history of alcohol abuse.
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spelling pubmed-60224342018-07-09 Rare variability in adrenoleukodystrophy: a case report Chen, Yanming Polara, Farhana Pillai, Anjana J Med Case Rep Case Report BACKGROUND: X-linked adrenoleukodystrophy is a genetic disorder with diverse clinical phenotypes. Of these phenotypes, the cerebral form usually manifests during early childhood with rapid cognitive and neurological deterioration and is accompanied by extensive white matter involvement. Adrenomyeloneuropathy, however, usually affects young adults and has focal symptoms typical of spinal cord and peripheral nerve involvement. CASE PRESENTATION: A 35-year-old African American man with a history of alcohol abuse presented with personality changes and lower extremity weakness. Diffuse demyelination was found on the brain image, and a diagnosis of the cerebral form was made based on the clinical features and genetic test. CONCLUSIONS: We report a rare case of adult-onset cerebral X-linked leukodystrophy with a clinical phenotype of adrenomyeloneuropathy, and the diagnosis was confounded by a history of alcohol abuse. BioMed Central 2018-06-28 /pmc/articles/PMC6022434/ /pubmed/29950168 http://dx.doi.org/10.1186/s13256-018-1722-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Chen, Yanming
Polara, Farhana
Pillai, Anjana
Rare variability in adrenoleukodystrophy: a case report
title Rare variability in adrenoleukodystrophy: a case report
title_full Rare variability in adrenoleukodystrophy: a case report
title_fullStr Rare variability in adrenoleukodystrophy: a case report
title_full_unstemmed Rare variability in adrenoleukodystrophy: a case report
title_short Rare variability in adrenoleukodystrophy: a case report
title_sort rare variability in adrenoleukodystrophy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022434/
https://www.ncbi.nlm.nih.gov/pubmed/29950168
http://dx.doi.org/10.1186/s13256-018-1722-z
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