Literature DB >> 6246837

Diagnosis of infantile neuroaxonal dystrophy by skin biopsy.

K Wisniewski, H M Wisniewski.   

Abstract

Skin biopsy with ultrastructural examination of cutaneous nerves showed dystrophic axons (spheroids), confirming a diagnosis of infantile neuroaxonal dystrophy. Independent of axonal changes, a few endoneurial and Schwann cells showed cytoplasmic inclusion bodies composed of structures similar to those seen in the spheroids.

Entities:  

Mesh：

Year:  1980        PMID： 6246837     DOI： 10.1002/ana.410070416

Source DB:  PubMed          Journal:  Ann Neurol        ISSN： 0364-5134            Impact factor:   10.422


  6 in total

1.  Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis.

Authors:  A Malandrini; G M Fabrizi; P Bartalucci; C Salvadori; G Berti; C Sabò; G C Guazzi
Journal:  Childs Nerv Syst       Date:  1996-03       Impact factor: 1.475

2.  Axonal pathology of the skin in infantile neuroaxonal dystrophy.

Authors:  S Kimura; Y Sasaki; I Warlo; H H Goebel
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

3.  Infantile neuroaxonal dystrophy in an albino girl. A cliniconeuropathologic study.

Authors:  K E Wisniewski; M Laure-Kamionowska; J Sher; J Pitter
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

4.  Aluminum-induced neurofibrillary changes in axons and dendrites.

Authors:  H M Wisniewski; J W Shek; S Gruca; J A Sturman
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

5.  Pathology of skeletal muscle and intramuscular nerves in infantile neuroaxonal dystrophy.

Authors:  T Miike; Y Ohtani; S Nishiyama; I Matsuda
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

Review 6.  Disorders of metal metabolism.

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

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