X-linked adrenoleukodystrophy

Authors

DOI:

https://doi.org/10.35381/s.v.v6i3.2274

Keywords:

Adrenoleukodystrophy, X chromosome, adrenal insufficiency. (Source, DeCS).

Abstract

Objective: To analyze X-linked Adrenoleukodystrophy. Method: In this research, a search for updated information was carried out in electronic databases such as Scielo, PubMed, Virtual Health Library, Google Scholar, among others. Results and conclusions: Adrenoleukodystrophy, although it is a rare entity, should be considered within the differential diagnoses in the context of adult patients with progressive or recurrent chronic neurological syndromes, mainly myelopathies without a clear cause and especially when there is an association with adrenal insufficiency. or there is some family history. In short, X-linked adrenoleukodystrophy presents a key mitochondrial dysfunction at the beginning of the pathological cascade, although it is classified within the group of peroxisomal diseases.

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References

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Published

2022-10-01

How to Cite

Viteri-Rodríguez, J. A., Enrriquez-Grijalva, M. F., Sacancela-Gabilanes, M. P., & Vasconez-Nina, J. A. (2022). X-linked adrenoleukodystrophy. Revista Arbitrada Interdisciplinaria De Ciencias De La Salud. Salud Y Vida, 6(3), 597–606. https://doi.org/10.35381/s.v.v6i3.2274

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