Article Text
Test yourself
A hill walker with long chains
Statistics from Altmetric.com
Footnotes
Contributors DPB conceived the idea and wrote the paper. VS undertook the molecular genetics analysis and interpretation. RNDS managed the patient and edited the paper.
Competing interests None.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed. This paper was reviewed by Jeremy Chataway, London, UK.
Read the full text or download the PDF:
Other content recommended for you
- Adrenoleukodystrophy: a forgotten diagnosis in children with primary Addison's disease
- Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with “Lorenzo’s oil”
- X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy
- Adult-onset adrenoleukodystrophy presenting with status epilepticus and psychosis
- The difficulty in diagnosing X linked adrenoleucodystrophy and the importance of identifying cerebral involvement
- ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism
- Psychiatric disease in an adolescent as a harbinger of cerebral X-linked adrenoleukodystrophy
- Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era
- X-linked adrenoleukodystrophy presenting as Addison’s disease
- A practical approach to diagnosing adult onset leukodystrophies