Literature DB >> 7998779

Phenotypic heterogeneity of an adult form of adrenoleukodystrophy in monozygotic twins.

G Sobue1, I Ueno-Natsukari, H Okamoto, T A Connell, I Aizawa, K Mizoguchi, M Honma, G Ishikawa, T Mitsuma, N Natsukari.   

Abstract

We describe genetically proven monozygotic twins with the adult form of adrenoleukodystrophy with significant phenotypic heterogeneity. Myeloneuropathy was common to both patients, but cognitive impairment and affective symptoms with extensive demyelination in the brain were prominent in the older twin, while adrenal insufficiency was predominant in the younger twin. The younger twin, however, exhibited affective symptoms similar to those displayed by his elder twin 10 years later. These findings suggest that nongenetic factors are important in determining the phenotypic variation of adrenoleukodystrophy gene.

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Year:  1994        PMID: 7998779     DOI: 10.1002/ana.410360617

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  12 in total

Review 1.  X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy.

Authors:  B M van Geel; J Assies; R J Wanders; P G Barth
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-07       Impact factor: 10.154

Review 2.  On the front of X-linked adrenoleukodystrophy.

Authors:  P Aubourg
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

3.  Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophy.

Authors:  V Feigenbaum; G Lombard-Platet; S Guidoux; C O Sarde; J L Mandel; P Aubourg
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

4.  ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.

Authors:  S Kemp; P A Mooyer; P A Bolhuis; B M van Geel; J L Mandel; P G Barth; P Aubourg; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

5.  Clinical and genetic aspects in twelve Korean patients with adrenomyeloneuropathy.

Authors:  Hyung Jun Park; Ha Young Shin; Hoon-Chul Kang; Byung-Ok Choi; Bum Chun Suh; Ho Jin Kim; Young-Chul Choi; Phil Hyu Lee; Seung Min Kim
Journal:  Yonsei Med J       Date:  2014-04-01       Impact factor: 2.759

Review 6.  Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural history.

Authors:  Stephan Kemp; Irene C Huffnagel; Gabor E Linthorst; Ronald J Wanders; Marc Engelen
Journal:  Nat Rev Endocrinol       Date:  2016-06-17       Impact factor: 43.330

7.  Genomic profiling identifies novel mutations and SNPs in ABCD1 gene: a molecular, biochemical and clinical analysis of X-ALD cases in India.

Authors:  Neeraj Kumar; Krishna Kant Taneja; Veena Kalra; Madhuri Behari; Satinder Aneja; Surendra Kumar Bansal
Journal:  PLoS One       Date:  2011-09-22       Impact factor: 3.240

8.  An ABCD1 Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree.

Authors:  Masoud Mehrpour; Faeze Gohari; Majid Zaki Dizaji; Ali Ahani; May Christine V Malicdan; Babak Behnam
Journal:  J Mol Genet Med       Date:  2016-06-19

9.  Modeling and rescue of defective blood-brain barrier function of induced brain microvascular endothelial cells from childhood cerebral adrenoleukodystrophy patients.

Authors:  Catherine A A Lee; Hannah S Seo; Anibal G Armien; Frank S Bates; Jakub Tolar; Samira M Azarin
Journal:  Fluids Barriers CNS       Date:  2018-04-04

10.  S149R, a novel mutation in the ABCD1 gene causing X-linked adrenoleukodystrophy.

Authors:  Fang Yan; Wenbo Wang; Hui Ying; Hongyu Li; Jing Chen; Chao Xu
Journal:  Oncotarget       Date:  2017-09-18
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