Rett syndrome: findings suggesting axonopathy and mitochondrial abnormalities
Abstract
We report the histopathologic findings of 3 sural nerve biopsies and 1 muscle biopsy from 3 patients with Rett syndrome. The 3 sural nerve biopsies demonstrated a few ultrastructural abnormalities, including the presence of many Pi-granules and mitochondrial changes in the cytoplasm of Schwann cells, occasional bands of Büngner and onion-bulb formations, and mitochondrial alterations in myelinated axons. Morphometric analysis disclosed reduction in the number of large myelinated fibers with normal densities in comparison to those of an age-matched normal control. Light microscopic examination of the biopsied muscle from a 6-year-old patient with Rett syndrome revealed the existence of many small, dark, angulated fibers with NADH-TR staining. Ultrastructural investigation of the muscle confirmed the presence of the dumbbell-shaped mitochondria. Peripheral nerve involvement and the possibility of mitochondrial abnormalities in Rett syndrome were suggested by the results.
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Energy-producing mitochondria have abnormal structure in RTT patient cells.
“Additionally, energy-producing mitochondria have abnormal structure in patient cells [23–26].”
From Rett syndrome: a neurological disorder with metabolic components (2018) · cites this paper as [25]
Cites
Neuropathology of Rett syndrome
Jellinger, K., Seitelberger, F., Opitz, J. M., & Reynolds, J. F. (1986) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320250528 · Cited by 115 · see citing works
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Rett syndrome: a neurological disorder with metabolic components
Kyle, S. M., Vashi, N., & Justice, M. J. (2018) · Open Biology · doi:10.1098/rsob.170216 · Cited by 213 · see citing works
Jin, L.-W., Horiuchi, M., Wulff, H., Liu, X.-B., Cortopassi, G. A., Erickson, J. D., & Maezawa, I. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2778-14.2015 · Cited by 88 · see citing works
“Patients with RTT showed abnormal mitochondrial morphology (Ruch et al., 1989; Wakai et al., 1990; Dotti et al., 1993; Cornford et al., 1994), enzymatic defects of the mitochondrial respiratory chain (Eeg-Olofsson et al., 1989; Coker and Melnyk, 1991; Heilstedt et al., 2002), and increased…”
Background
- Authors
- Wakai, S., Kameda, K., Ishikawa, Y., Miyamoto, S., Nagaoka, M., Okabe, M., Minami, R., & Tachi, N.
- Affiliations
- Sapporo Medical University (JP)
- Corresponding author
- Wakai, Shuji
- Venue
- Pediatric Neurology
- Publisher
- Elsevier BV
- Published
- 1990-09
- Volume
- 6
- Issue
- 5
- Pages
- 339-343
- ISSN
- 0887-8994 (ISSN-L)
- OpenAlex
- W2032595150
- Cited by
- 48
- References
- 1
- Citations by year
- 2025: 4 · 2024: 1 · 2023: 1 · 2021: 5 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 4 · 2016: 2 · 2015: 2 · 2014: 1 · 2013: 1 · 2012: 2
- FWCI
- 1.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Pediatric Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- Rett syndrome, axonopathy, mitochondrial abnormalities, sural nerve biopsy, muscle biopsy, Schwann cells, onion bulb formation, myelinated axons, morphometrics, peripheral nerve involvement
- MeSH terms
- Axons, Biopsy, Child, Female, Humans, Mitochondria, Mitochondria, Muscle, Muscles, Nerve Fibers, Myelinated, Schwann Cells, Sural Nerve, Rett Syndrome
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