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Congenital spongiform leukodystrophy in 2 female littermate German shepherd puppies.
De Miguel, Ricardo; Hague, Devon Wallis; Johnson, Jennifer L; Zilinger, Amber M; Kukekova, Anna; Lezmi, Stephane.
Afiliación
  • De Miguel R; AnaPath Services GmbH, Liestal, Switzerland.
  • Hague DW; Department of Veterinary Clinical Medicine, University of Illinois, Urbana, Illinois, USA.
  • Johnson JL; Department of Animal Sciences, College of Agricultural, Consumer and Environmental Sciences, University of Illinois at Urbana-Champaign, Champaign, Illinois, USA.
  • Zilinger AM; Department of Animal Sciences, College of Agricultural, Consumer and Environmental Sciences, University of Illinois at Urbana-Champaign, Champaign, Illinois, USA.
  • Kukekova A; Department of Animal Sciences, College of Agricultural, Consumer and Environmental Sciences, University of Illinois at Urbana-Champaign, Champaign, Illinois, USA.
  • Lezmi S; Department of Pathobiology, University of Illinois at Urbana-Champaign, Champaign, Illinois, USA.
J Vet Intern Med ; 38(3): 1730-1736, 2024.
Article en En | MEDLINE | ID: mdl-38544400
ABSTRACT
Two 9-week-old female littermate German Shepherd puppies showed severe high-frequency low-amplitude trembling that worsened with movement. The white matter (WM) of the central nervous system (CNS) showed bilateral diffuse severe spongiosis in the cerebellum, brainstem, spinal cord, and the neuropil of the oculomotor and red nuclei. The cortical corona radiata was less severely affected. Rare necrotic or apoptotic glia-like cells also were identified in the WM. Luxol fast blue staining disclosed severe diffuse myelin loss in the entire CNS; peripheral nerves were spared. Glial fibrillary acidic protein immunohistochemistry showed diffuse astrogliosis and astrocytosis in the WM. Genetic analyses of the littermates excluded the aspartoacylase (ASPA) gene as a candidate for this condition in dogs. In conclusion, this description of a rare congenital spongiform leukodystrophy in the German Shepherd breed, closely resembling to Canavan disease in humans, is likely caused by a genetic alteration unrelated to the ASPA gene.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de los Perros Límite: Animals Idioma: En Revista: J Vet Intern Med Asunto de la revista: MEDICINA INTERNA / MEDICINA VETERINARIA Año: 2024 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de los Perros Límite: Animals Idioma: En Revista: J Vet Intern Med Asunto de la revista: MEDICINA INTERNA / MEDICINA VETERINARIA Año: 2024 Tipo del documento: Article País de afiliación: Suiza