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Suspected malnutrition-induced reversible feline skin fragility syndrome in a cat with congenital axial deformities.

Authors :
Yu Y
Miyamoto T
Kimura Y
Itamoto K
Michishita M
Hatakeyama H
Nagashima T
Asada R
Yamaguchi T
Hasegawa D
Nomura Y
Lyons LA
Kosho T
Source :
The Canadian veterinary journal = La revue veterinaire canadienne [Can Vet J] 2024 Mar; Vol. 65 (3), pp. 227-233.
Publication Year :
2024

Abstract

A stray cat, an intact female Japanese domestic shorthair cat of unknown age (suspected to be a young adult), was rescued. The cat was lethargic and thin and had marked skin fragility, delayed wound healing without skin hyperextensibility, and hind limb proprioceptive ataxia and paresis. Survey radiography, computed tomography, and magnetic resonance imaging revealed congenital vertebral anomalies, including thoracolumbar transitional vertebrae, scoliosis resulting from a thoracic lateral wedge-shaped vertebra, and a kinked tail, and a dilated spinal cord central canal. Through nutritional support, the cat's general condition normalized, followed by a gradual and complete improvement of skin features. Whole-genome sequencing was completed; however, no pathogenic genetic variant was identified that could have caused this phenotype, including congenital scoliosis. A skin biopsy obtained 7 y after the rescue revealed no remarkable findings on histopathology or transmission electron microscopy. Based on clinical course and microscopic findings, malnutrition-induced reversible feline skin fragility syndrome (FSFS) was suspected, and nutritional support was considered to have improved the skin condition. Key clinical message: This is the second reported case of presumed malnutrition-induced reversible FSFS and was accompanied by long-term follow-up.<br /> (Copyright and/or publishing rights held by the Canadian Veterinary Medical Association.)

Details

Language :
English
ISSN :
0008-5286
Volume :
65
Issue :
3
Database :
MEDLINE
Journal :
The Canadian veterinary journal = La revue veterinaire canadienne
Publication Type :
Report
Accession number :
38434166