The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Small nerve fiber involvement is frequent in X-linked adrenoleukodystrophy
Abstract
OBJECTIVE: To investigate the presence of small nerve fiber dysfunction in subjects with X-linked adrenoleukodystrophy. METHODS: Cross-sectional study in which 11 Norwegian subjects (3 males, 8 females) with X-linked adrenoleukodystrophy, phenotypes ranging from asymptomatic to wheelchair-bound with adrenomyeloneuropathy, were investigated with neurophysiologic studies including EMG, nerve conduction velocities, quantitative sensory testing, tests of autonomic function, and skin biopsy for intraepidermal nerve fiber density measurements. RESULTS: We found small nerve fiber dysfunction in 10 of 11 subjects, increasing with age and more pronounced in males. Low intraepidermal nerve fiber densities were found in 5 of 11 subjects, indicating a loss of thin unmyelinated nerve fibers peripherally. Five of 11 subjects showed small nerve fiber dysfunction despite normal nerve fiber densities, suggesting possible involvement of the spinothalamic tracts. Two subjects showed moderate abnormalities in autonomic function tests. CONCLUSIONS: Evidence of small nerve fiber dysfunction was widespread in this cohort of subjects with X-linked adrenoleukodystrophy, with findings indicating loss of peripheral small nerve fibers and possibly also fibers of the spinothalamic tracts. The results support the theory of primary axonal degeneration in adrenomyeloneuropathy. Evidence of nervous system involvement was found in all heterozygotes, with severity increasing with age. Clinicians caring for these patients should be alert to signs of small nerve fiber involvement.
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“Female patients with ALD remain asymptomatic in childhood and adolescence, while in adulthood, myeloneuropathy symptoms can arise.7,14”
From International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy (2022) · cites this paper as [14]
In the citing paper
“Peripheral neuropathy is a common feature of ALD but is rarely the presenting symptom.7,14-16”
From International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy (2022) · cites this paper as [14]
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Adrenoleukodystrophy—Neuroendocrine pathogenesis and redefinition of natural history
Kemp, S., Huffnagel, I. C., Linthorst, G. E., Wanders, R. J., & Engelen, M. (2016) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2016.90 · Cited by 275
X-Linked Adrenoleukodystrophy: Pathogenesis and Treatment
Engelen, M., Kemp, S., & Poll-The, B.-T. (2014) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-014-0486-0 · Cited by 187
International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy
Engelen, M., van Ballegoij, W. J. C., Mallack, E. J., Van Haren, K. P., Köhler, W., Salsano, E., van Trotsenburg, A. S. P., Mochel, F., Sevin, C., Regelmann, M. O., et al. (2022) · Neurology · doi:10.1212/wnl.0000000000201374 · Cited by 156
“Female patients with ALD remain asymptomatic in childhood and adolescence, while in adulthood, myeloneuropathy symptoms can arise.(7,14) Cerebral ALD and primary adrenal insufficiency are extremely rare in women.”
BackgroundThe pathology of X-linked adrenoleukodystrophy: Tissue specific changes as a clue to pathophysiology
Yska, H. A. F., Engelen, M., & Bugiani, M. (2024) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-024-03105-0 · Cited by 20
“Apart from these theories, it has been postulated that VLCFA accumulation alone may not be the only causative agent of ALD.”
Background
Metadata
- Authors
- Horn, M. A., Nilsen, K. B., Jørum, E., Mellgren, S. I., & Tallaksen, C. M. E.
- Affiliations
- Oslo University Hospital (NO)
- Venue
- Neurology
- Published
- 2014-05-13
- Volume
- 82
- Issue
- 19
- Pages
- 1678-1683
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W1975702675
- Cited by
- 21
- References
- 2
- Citations by year
- 2025: 1 · 2024: 5 · 2023: 1 · 2022: 2 · 2021: 1 · 2019: 1 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 1 · 2014: 3
- FWCI
- 1.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Health Sciences › Medicine › Clinical Neurology › Peripheral Neuropathies and Disorders
- Keywords
- X-linked adrenoleukodystrophy, adrenomyeloneuropathy, intraepidermal nerve fiber density, unmyelinated nerve fibers, spinothalamic tract, autonomic dysfunction, axonal degeneration, heterozygotes, quantitative sensory testing
- MeSH terms
- Adrenoleukodystrophy, Age Factors, Aged, Autonomic Nervous System, Cross-Sectional Studies, Epidermis, Erythromelalgia, Female, Humans, Male, Middle Aged, Nerve Degeneration, Neural Conduction, Sex Characteristics
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