Literature DB >> 1574990

Screening of patients with hereditary spastic paraparesis and Addison's disease for adrenoleukodystrophy/adrenomyeloneuropathy.

B H Holmberg1, E Hägg, M Duchek, L Hagenfeldt.   

Abstract

X-linked adrenoleukodystrophy/adrenomyeloneuropathy presents a wide variation of clinical manifestations and may mimic several diseases. A screening investigation by measuring plasma saturated very long-chain fatty acids was performed in two groups of patients. Among six patients with hereditary spastic paraparesis one woman was detected to be a heterozygous gene carrier. However, in a group of eleven adult men with idiopathic Addison's disease the plasma concentrations of very long-chain fatty acids were all within normal limits. We conclude that X-linked adrenoleukodystrophy and symptomatic heterozygous females should be considered in cases of progressive spastic paraparesis.

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Year:  1992        PMID: 1574990     DOI: 10.1111/j.1600-0404.1992.tb04015.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  2 in total

Review 1.  Adrenomyeloneuropathy as a cause of primary adrenal insufficiency and spastic paraparesis.

Authors:  Monika Spurek; Regina Taylor-Gjevre; Stan Van Uum; Hasnain M Khandwala
Journal:  CMAJ       Date:  2004-10-26       Impact factor: 8.262

2.  X-linked adrenoleukodystrophy in patients with idiopathic Addison disease.

Authors:  P Jorge; D Quelhas; P Oliveira; R Pinto; A Nogueira
Journal:  Eur J Pediatr       Date:  1994-08       Impact factor: 3.183

  2 in total

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