Sporadic adult-onset leucodystrophy with axonal spheroids and pigmented glia with no mutations in the known targeted genes

Author:

Fernández-Vega Ivan12ORCID,Pérez de Heredia-Goñi Katti2,Santos-Juanes Jorge3,Goñi Imizcoz Miguel4,Zaldumbide Laura5,Zarranz Juan Jose6,Ferrer Isidro7

Affiliation:

1. Pathology Department of Hospital Universitario Araba; Álava Spain

2. Brain Bank Hospital Universitario Araba; Biobanco Vasco para la Investigación (O+eHun); Vitoria Spain

3. Pathology Department; Hospital Universitario Central de Asturias; Asturias Spain

4. Neurology Department; Hospital Divino Vallés; Burgos Spain

5. Pathology Department of Hospital Universitario de Cruces; Bizkaia Spain

6. Neurology Department; Hospital Universitario de Cruces; Bizkaia Spain

7. Institute of Neuropathology; Bellvitge University Hospital; University of Barcelona; Barcelona Spain

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Reference42 articles.

1. Ludo van Bogaert (1897-1989);Martin;Acta Neurol. Belg.,1996

2. Pigmentary type of orthochromatic leukodystrophy (old): a new case with ultrastructural and biochemical study;Gray;J. Neuropathol. Exp. Neurol.,1987

3. Leucodystrophy with pigmented glial and scavenger cells (pigmentary type of orthochromatic leucodystrophy);Tunon;Neuropathol. Appl. Neurobiol.,1988

4. The dominant form of the pigmentary orthochromatic leukodystrophy;Constantinidis;Acta Neuropathol.,1991

5. A rare form of adult onset leukodystrophy: orthochromatic leukodystrophy with pigmented glia;Shannon;Can. J. Neurol. Sci.,1997

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