Literature DB >> 21115380

Fucosidosis in a domestic shorthair cat.

Lorna P Arrol1, Annette M Kerrins, Yoshika Yamakawa, Peter M Smith.   

Abstract

This paper documents the first reported case of fucosidosis in a cat. The cat presented with signs of forebrain and cerebellar dysfunction and a magnetic resonance imaging scan of the brain suggested a degenerative or metabolic disease process. A fine needle aspirate of grossly normal lymph nodes revealed vacuolated lymphocytes and a renal biopsy of an irregular shaped kidney identified vacuolated tubular epithelial cells. A white cell lysosomal enzyme screen revealed negligible α-fucosidase activity. Fucosidosis should be considered in the differential diagnosis of young cats with cerebellar dysfunction and must be added to the list of lysosomal storage diseases affecting the cat.
Copyright © 2010 ISFM and AAFP. Published by Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21115380     DOI: 10.1016/j.jfms.2010.09.001

Source DB:  PubMed          Journal:  J Feline Med Surg        ISSN: 1098-612X            Impact factor:   2.015


  4 in total

1.  Dried blood spots for the enzymatic diagnosis of lysosomal storage diseases in dogs and cats.

Authors:  Adrian C Sewell; Mark E Haskins; Urs Giger
Journal:  Vet Clin Pathol       Date:  2012-11-02       Impact factor: 1.180

2.  Magnetic resonance findings of the corpus callosum in canine and feline lysosomal storage diseases.

Authors:  Daisuke Hasegawa; Shinji Tamura; Yuya Nakamoto; Naoaki Matsuki; Kimimasa Takahashi; Michio Fujita; Kazuyuki Uchida; Osamu Yamato
Journal:  PLoS One       Date:  2013-12-27       Impact factor: 3.240

3.  A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease.

Authors:  Heike Wolf; Markus Damme; Stijn Stroobants; Rudi D'Hooge; Hans Christian Beck; Irm Hermans-Borgmeyer; Renate Lüllmann-Rauch; Thomas Dierks; Torben Lübke
Journal:  Dis Model Mech       Date:  2016-08-04       Impact factor: 5.758

4.  The Value of Case Reports in Systematic Reviews from Rare Diseases. The Example of Enzyme Replacement Therapy (ERT) in Patients with Mucopolysaccharidosis Type II (MPS-II).

Authors:  Miguel Sampayo-Cordero; Bernat Miguel-Huguet; Andrea Malfettone; José Manuel Pérez-García; Antonio Llombart-Cussac; Javier Cortés; Almudena Pardo; Jordi Pérez-López
Journal:  Int J Environ Res Public Health       Date:  2020-09-10       Impact factor: 3.390

  4 in total

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