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pubmed-article:1528022pubmed:abstractTextThe adrenoleukodystrophies refer to three genetically distinct disorders all characterized by the accumulation of very long-chain fatty acids. In this paper we will review the biochemical aspects of these leukodystrophies with particular emphasis on the methods used to measure very long-chain fatty acid levels in plasma and their reliability. Furthermore, we will concentrate on the primary defect in the X-linked form of adrenoleukodystrophy.lld:pubmed
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pubmed-article:1528022pubmed:articleTitleX-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect.lld:pubmed
pubmed-article:1528022pubmed:affiliationDepartment of Pediatrics, University Hospital of Amsterdam, The Netherlands.lld:pubmed
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