Literature DB >> 4013671

Histological and ultrastructural features of dystrophic isocortical axons in infantile neuroaxonal dystrophy (Seitelberger's disease).

G A de León, M H Mitchell.   

Abstract

The histological and ultrastructural features of axonal swellings are described in a cerebral biopsy specimen from a 6-year-old girl with infantile neuroaxonal dystrophy. In agreement with previous reports, several swellings were identified as axonal terminals, and it is postulated that the prevailing axonal swellings in cerebral cortex represent dystrophic boutons. Microscopically, dystrophic cortical boutons are morphologically different from typical subcortical spheroids and can be easily identified in routine histological preparations. Five ultrastructural elements were present in most axonal swellings: clusters of characteristic membranous bodies, stacks of elongated membranes, mitochondria, groups of vesicles, and an amorphous matrix. In spite of widespread axonal enlargement, the cerebral cortex was not thickened, and, in fact, the gyri looked atrophic in computerized axial tomograms. These findings suggest that some normal cortical element must be deficient, but such a structure remains to be identified.

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Year:  1985        PMID: 4013671     DOI: 10.1007/bf00688682

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  12 in total

1.  Infantile neuroaxonal dystrophy. An electron microscopic study of a case clinically resembling neuronal ceroid-lipofuscinosis.

Authors:  J F Butzer; S S Schochet; W E Bell
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

2.  [INFANTILE NEURO-AXONAL DEGENERATION (SEITELBERGER'S DISEASE). ANATOMICAL STUDY OF A CASE].

Authors:  G LYON; G SEE
Journal:  Rev Neurol (Paris)       Date:  1963-08       Impact factor: 2.607

3.  Infantile neuroaxonal dystrophy.

Authors:  D COWEN; E V OLMSTEAD
Journal:  J Neuropathol Exp Neurol       Date:  1963-04       Impact factor: 3.685

4.  Infantile neuroaxonal dystrophy: cortical axonic and presynaptic changes.

Authors:  U Sandbank; P Lerman; M Geifman
Journal:  Acta Neuropathol       Date:  1970       Impact factor: 17.088

5.  Infantile neuroaxonal dystrophy. A disease characterized by altered terminal axons and synaptic endings.

Authors:  E T Hedley-Whyte; F H Gilles; B G Uzman
Journal:  Neurology       Date:  1968-09       Impact factor: 9.910

6.  Electron microscopic observations in infantile neuroaxonal dystrophy. Report of a cortical biopsy and review of the recent literature.

Authors:  M M Herman; P R Huttenlocher; K G Bensch
Journal:  Arch Neurol       Date:  1969-01

7.  An analysis of the ultrastructural findings in infantile neuroaxonal dystrophy (Seitelberger's disease).

Authors:  H M Liu; M Larson; Y Mizuno
Journal:  Acta Neuropathol       Date:  1974-03-26       Impact factor: 17.088

8.  Altered axons and axon terminals in the lateral vestibular nucleus of the rat. Possible example of axonal remodeling.

Authors:  C Sotelo; S L Palay
Journal:  Lab Invest       Date:  1971-12       Impact factor: 5.662

9.  Infantile neuroaxonal dystrophy with neonatal onset. Neuropathologic and electron microscopic observations.

Authors:  S Kamoshita; H B Neustein; B H Landing
Journal:  J Neuropathol Exp Neurol       Date:  1968-04       Impact factor: 3.685

10.  Unusual neocortical presynaptic terminals in a patient with convulsions, mental retardation and cortical blindness: an electron microscopic study.

Authors:  N K Gonatas; E S Goldehsohn
Journal:  J Neuropathol Exp Neurol       Date:  1965-10       Impact factor: 3.685

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  5 in total

1.  Congenital Pick cell encephalopathy: a distinct disorder characterized by diffuse formation of Pick cells in the cerebral cortex.

Authors:  G A de León; G Breningstall; N Zaeri
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

2.  Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations.

Authors:  Ibrahim Malik; John Turk; David J Mancuso; Laura Montier; Mary Wohltmann; David F Wozniak; Robert E Schmidt; Richard W Gross; Paul T Kotzbauer
Journal:  Am J Pathol       Date:  2008-01-17       Impact factor: 4.307

3.  Catalytic function of PLA2G6 is impaired by mutations associated with infantile neuroaxonal dystrophy but not dystonia-parkinsonism.

Authors:  Laura A Engel; Zheng Jing; Daniel E O'Brien; Mengyang Sun; Paul T Kotzbauer
Journal:  PLoS One       Date:  2010-09-23       Impact factor: 3.240

4.  Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy.

Authors:  A Malandrini; T Cavallaro; G M Fabrizi; G Berti; R Salvestroni; C Salvadori; G C Guazzi
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064

5.  Ultrastructural features of canine neuroaxonal dystrophy in a Papillon dog.

Authors:  Miyuu Tanaka; Shinobu Yamaguchi; Hideo Akiyoshi; Masaya Tsuboi; Kazuyuki Uchida; Takeshi Izawa; Jyoji Yamate; Mitsuru Kuwamura
Journal:  J Vet Med Sci       Date:  2017-10-10       Impact factor: 1.267

  5 in total

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