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Adrenomyeloneuropathy as a form of presentation of adrenoleukodystrophy: Case report

dc.contributor.authorLadera-Córdova, M.
dc.contributor.authorCondori-Chacón, C.
dc.contributor.authorRivera-Torrejón, O.
dc.contributor.authorAlva-Díaz, C.
dc.contributor.authorVásquez Quicaño, K.
dc.contributor.authorTerreros Palomino, A.
dc.contributor.authorMori-Quispe, N.
dc.contributor.authorShchegolikhina, U.
dc.contributor.authorRomero-Sánchez, R.
dc.contributor.authorPacheco-Barrios, K.
dc.date.accessioned2025-10-31T18:32:19Z
dc.date.available2025-10-31T18:32:19Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/20.500.12805/4587
dc.description.abstractIntroduction: Adrenomyeloneuropathy is one of the manifestations of adrenoleukodystrophy-X, which is found within the 6 phenotypes of this neurodegenerative disorder. Case report: A 42-year-old male started the symptoms 22 years ago, characterized by a progressive paraparesis and difficulty in march, continuing in adulthood with gingival and mamilar hyperpigmentation, spastic paraparesis and hyperreflexia. The magnetic resonance of the spine showed alteration at the level of T2-T7, establishing the diagnosis by higher plasmatic values of very long chain fatty acids. Conclusions: A case of adrenomyeloneuropathy is reported in Peru that meets the clinical, imaging and laboratory criteria.en_US
dc.formatapplication/pdf
dc.language.isoeng
dc.language.isospa
dc.publisherEdiciones Doyma
dc.relation.ispartofurn:issn:1853-0028
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectTherapeutic Advances in Lysosomal Storage Disordersen_US
dc.subjectAdrenoleukodystrophy: Genetic Insights and Imaging Advancesen_US
dc.titleAdrenomyeloneuropathy as a form of presentation of adrenoleukodystrophy: Case reporten_US
dc.typehttps://purl.org/coar/resource_type/c_0857
dc.identifier.doihttps://doi.org/10.1016/j.neuarg.2020.09.003
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.25
dc.type.otherCommunication letter o Case Report
dc.identifier.journalNeurologia Argentina
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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