Literature DB >> 10068516

Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophy.

C D Boehm1, G R Cutting, M B Lachtermacher, H W Moser, S S Chong.   

Abstract

X-linked adrenoleukodystrophy is a serious and often fatal disorder, affecting the white matter of the nervous system, the adrenal cortex, and the testis. The gene mutated in X-ALD encodes a peroxisomal membrane protein, ALDP. The presence of very long chain fatty acids in plasma is highly diagnostic for affected males and carrier females, but exclusion of carrier status biochemically is unreliable. Molecular analysis of the X-ALD gene has the potential to either identify or rule out carrier status accurately, but is complicated by the existence of autosomal paralogs. We have developed and validated a robust DNA diagnostic test for this disorder involving nonnested genomic amplification of the X-ALD gene, followed by fluorescent dye-primer sequencing and analysis. This protocol provides a highly reliable means of determining carrier status in women at risk for transmitting X-ALD and is applicable to a clinical diagnostic laboratory. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10068516     DOI: 10.1006/mgme.1998.2779

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  24 in total

1.  CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR.

Authors:  Molly B Sheridan; Timothy W Hefferon; Nulang Wang; Christian Merlo; Carlos Milla; Drucy Borowitz; Eric D Green; Peter J Mogayzel; Garry R Cutting
Journal:  J Med Genet       Date:  2010-11-20       Impact factor: 6.318

2.  A Novel Double Mutation in the ABCD1 Gene in a Patient with X-linked Adrenoleukodystrophy: Analysis of the Stability and Function of the Mutant ABCD1 Protein.

Authors:  Masashi Morita; Junpei Kobayashi; Kozue Yamazaki; Kosuke Kawaguchi; Ayako Honda; Kenji Sugai; Nobuyuki Shimozawa; Reiji Koide; Tsuneo Imanaka
Journal:  JIMD Rep       Date:  2013-02-12

3.  A novel missense mutation in the ABCD1 gene of a Chinese boy diagnosed with X-linked adrenoleukodystrophy: case report.

Authors:  Mengqi Zhang; Shupeng Shi; Haoran Zhang; Lihui Liu; Linchao Wu; Bo Xiao; Weiping Liu
Journal:  Neurol Sci       Date:  2018-10-20       Impact factor: 3.307

4.  Clinical reasoning: a 56-year-old man with progressive spasticity.

Authors:  Radhika Dhamija; Gerald V Raymond; Ralitza Gavrilova
Journal:  Neurology       Date:  2013-02-26       Impact factor: 9.910

5.  Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.

Authors:  Deyanira Corzo; William Gibson; Kisha Johnson; Grant Mitchell; Guy LePage; Gerald F Cox; Robin Casey; Carolyn Zeiss; Heidi Tyson; Garry R Cutting; Gerald V Raymond; Kirby D Smith; Paul A Watkins; Ann B Moser; Hugo W Moser; Steven J Steinberg
Journal:  Am J Hum Genet       Date:  2002-04-29       Impact factor: 11.025

6.  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

7.  The impact of a ketogenic diet and liver dysfunction on serum very long-chain fatty acids levels.

Authors:  T J Stradomska; M Bachański; J Pawłowska; M Syczewska; A Stolarczyk; A Tylki-Szymańska
Journal:  Lipids       Date:  2013-01-31       Impact factor: 1.880

Review 8.  Therapy of X-linked adrenoleukodystrophy.

Authors:  Hugo W Moser
Journal:  NeuroRx       Date:  2006-04

Review 9.  "Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: rationale and current assessment of efficacy.

Authors:  Hugo W Moser; Ann B Moser; Kim Hollandsworth; N Hong Brereton; Gerald V Raymond
Journal:  J Mol Neurosci       Date:  2007-09       Impact factor: 3.444

Review 10.  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

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