Literature DB >> 2059251

Terminal axon pathology in infantile neuroaxonal dystrophy.

S Kimura1.   

Abstract

In order to clarify the pathogenesis of infantile neuroaxonal dystrophy, ultrastructural studies of the terminal and nonterminal axons of motor and autonomic nerves in muscle and skin, of which structures are much simpler than those of the central nervous system, were performed in 5 patients affected by infantile neuroaxonal dystrophy. The primary lesion was located in the axon terminal; the majority of terminal axons were dystrophic with tubulo-membranous profiles, while there were only a few dystrophic axons in the nonterminal axons. According to these findings, it is logical to consider that interruption of axonal transport at the site of the "turnaround" process is a cause of dystrophic change of the terminal axon in infantile neuroaxonal dystrophy.

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Year:  1991        PMID: 2059251     DOI: 10.1016/0887-8994(91)90007-8

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  5 in total

1.  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

2.  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

Review 3.  Brain, blood, and iron: perspectives on the roles of erythrocytes and iron in neurodegeneration.

Authors:  Rainer Prohaska; Ody C M Sibon; Dobrila D Rudnicki; Adrian Danek; Susan J Hayflick; Esther M Verhaag; Jan J Vonk; Russell L Margolis; Ruth H Walker
Journal:  Neurobiol Dis       Date:  2012-03-09       Impact factor: 5.996

Review 4.  Disorders of metal metabolism.

Authors:  Carlos R Ferreira; William A Gahl
Journal:  Transl Sci Rare Dis       Date:  2017-12-18

Review 5.  Defective lipid metabolism in neurodegeneration with brain iron accumulation (NBIA) syndromes: not only a matter of iron.

Authors:  Cristina Colombelli; Manar Aoun; Valeria Tiranti
Journal:  J Inherit Metab Dis       Date:  2014-10-10       Impact factor: 4.982

  5 in total

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