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A case of female adrenoleukodystrophy carrier with insidious neurogenic bladder.
Obara, Koji; Abe, Erika; Shimozawa, Nobuyuki; Toyoshima, Itaru.
Afiliación
  • Obara K; Department of Neurology National Hospital Organization Akita National Hospital Yurihonjo Japan.
  • Abe E; Department of Neurology National Hospital Organization Akita National Hospital Yurihonjo Japan.
  • Shimozawa N; Division of Genomics Research Life Science Research Center Gifu University Gifu Japan.
  • Toyoshima I; Department of Neurology National Hospital Organization Akita National Hospital Yurihonjo Japan.
J Gen Fam Med ; 21(4): 146-147, 2020 Jul.
Article en En | MEDLINE | ID: mdl-32742905
ABSTRACT
A 65-year-old woman with mutation of the ABCD1 gene for adrenoleukodystrophy (ALD) was admitted to our hospital with a urinary tract infection. Abdominal computed tomography showed dilation of the urinary tract. Although she had noticed pollakisuria since her forties, she had not been followed up by any medical institutions until we diagnosed her as a female carrier with ALD. ALD is an X-linked pattern of inheritance that typically affects males, but many female carriers actually present slowly progressive myelopathy and neuropathy. Therefore, it is important to identify female carriers with ALD and treat them at the earliest stage possible.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Gen Fam Med Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Gen Fam Med Año: 2020 Tipo del documento: Article