Literature DB >> 3087188

Neuropathology of Rett syndrome.

K Jellinger, F Seitelberger.   

Abstract

Autopsy studies in 8 girls with the Rett syndrome dying between 4 and 15 years showed: Diffuse cerebral atrophy/micrencephaly, with a decrease in brain weight by 13.8 to 33.8% of age-matched controls, apparently related to the duration of the disorder; Mild, but inconsistent diffuse cortical atrophy without developmental disorders apart from occasional microdysgenesis (three cases), but increased amounts of neuronal lipofuscin, and occasional mild astrocytic gliosis; Mild, but inconsistent spongy changes in cerebral and cerebellar white matter, optic nerve (two cases), and myelinated fascicles of the brainstem tegmentum, without signs of dys- or demyelination, and apparently different from the spongy myelinopathy common to aminoacidopathies; Most conspicuous was an underpigmentation of the substantia nigra which contained many fewer well-pigmented neurons for age (53-73%), and fewer pigmented granules per neuron, while the total number of nigral neurons and the triphasic substructure of neuromelanin were normal for age. No pathologic changes were seen in locus coeruleus, nucleus basalis of Meynert, and nucleus dorsalis raphe; Electron microscopy of autopsy material from an 11-year-old girl showed increased amounts of neuronal lipofuscin without signs of a storage disorder. Reactive and degenerating axons in the caudate nucleus were possibly related to the nigral changes, suggesting some dysfunction of the dopaminergic nigro-striatal system, while the synaptic organization of the neostriatum appeared unaffected. Peripheral nerve from a patient dying in advanced stage showed increased numbers of unmyelinated (regenerated?) axons, with almost no demyelination and few remyelinated axons, suggesting axonal degeneration rather than hypomyelination, but exogenous factors (malnutrition) cannot be excluded. The pathogenetic mechanisms of the morphologic brain lesions and their relations to clinical and neurochemical findings in Rett syndrome are unknown and deserve further intensive investigations.

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Year:  1986        PMID: 3087188     DOI: 10.1002/ajmg.1320250528

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  17 in total

Review 1.  Complexities of Rett syndrome and MeCP2.

Authors:  Rodney C Samaco; Jeffrey L Neul
Journal:  J Neurosci       Date:  2011-06-01       Impact factor: 6.167

Review 2.  Rett syndrome and MeCP2: linking epigenetics and neuronal function.

Authors:  Mona D Shahbazian; Huda Y Zoghbi
Journal:  Am J Hum Genet       Date:  2002-11-19       Impact factor: 11.025

3.  Neurophysiological observations on corticospinal projections to the upper limb in subjects with Rett syndrome.

Authors:  J A Eyre; A M Kerr; S Miller; M C O'Sullivan; V Ramesh
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-10       Impact factor: 10.154

Review 4.  Rett syndrome: a review of current knowledge.

Authors:  R Van Acker
Journal:  J Autism Dev Disord       Date:  1991-12

5.  Neuropathology of Rett syndrome.

Authors:  K Jellinger; D Armstrong; H Y Zoghbi; A K Percy
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

Review 6.  Brief report: neuroanatomic observations of the brain in pervasive developmental disorders.

Authors:  M L Bauman
Journal:  J Autism Dev Disord       Date:  1996-04

Review 7.  Rett syndrome.

Authors:  A Clarke
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

8.  Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.

Authors:  Meagan R Pitcher; José A Herrera; Shelly A Buffington; Mikhail Y Kochukov; Jonathan K Merritt; Amanda R Fisher; N Carolyn Schanen; Mauro Costa-Mattioli; Jeffrey L Neul
Journal:  Hum Mol Genet       Date:  2015-01-29       Impact factor: 6.150

9.  MeCP2 reinforces STAT3 signaling and the generation of effector CD4+ T cells by promoting miR-124-mediated suppression of SOCS5.

Authors:  Shan Jiang; Chaoran Li; Gabrielle McRae; Erik Lykken; Jose Sevilla; Si-Qi Liu; Ying Wan; Qi-Jing Li
Journal:  Sci Signal       Date:  2014-03-11       Impact factor: 8.192

10.  Reduced concentrations and increased metabolism of biogenic amines in a single case of Rett-syndrome: a postmortem brain study.

Authors:  T Brücke; E Sofic; W Killian; A Rett; P Riederer
Journal:  J Neural Transm       Date:  1987       Impact factor: 3.575

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